The Recall Desk

Archive

August 2023 recalls

693 recalls were announced in August 2023.

What the numbers show

Critical
15
Severe
87
High
526
Moderate
65

Of the 693 recalls this month scored against our rubric, 2% are Critical, 13% are Severe.

Which agencies issued them

101–200 of 693

  • SevereFDA (Devices)·Z-2368-2023·2023-08-23

    Dialysis Catheter Recalled Due to Excessive Lubricant Causing Center Lumen Obstruction

    Covidien is recalling MAHURKAR dialysis catheters due to excessive silicone-based lubricant coating the center lumen tip, which may cause partial or complete obstruction, delaying treatment or causing thrombosis.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 16 cm, Curved Extensions, IC Tray REF: 8888101002HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2375-2023·2023-08-23

    Dialysis catheter recalled due to excessive lubricant causing obstruction

    Covidien's MAHURKAR dialysis catheter is recalled because excessive silicone lubricant can block the center lumen, preventing or reducing blood flow during dialysis. This Class I recall affects 271 units and carries risk of treatment delays, hemolysis, and blood clots.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Curved Extensions, PASS Tray REF: 8888103004HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23T005000·2023-08-23

    Yokohama Recalls 504C Tires Due to Sidewall Air Leak Risk

    Yokohama is recalling 6,992 specific 504C tires because a defective splice may allow air to leak into the sidewall, potentially causing a crash.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2385-2023·2023-08-23

    Acute Dialysis Catheter Recalled for Potential Lumen Obstruction and Embolism Risk

    Covidien is recalling MAHURKAR acute dialysis catheters for excessive silicone lubricant causing lumen obstruction that may delay treatment and lead to hemolysis, embolism, or thrombosis.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, Kit REF: 8888345603HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2391-2023·2023-08-23

    Dialysis Catheter Recalled for Center Lumen Occlusion Risk

    Covidien LP is recalling 3,965 MAHURKAR dialysis catheters due to excessive lubricant causing center lumen occlusion. This may obstruct blood flow or cause hemolysis and blood clots.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Curved Extensions, Kit REF: 8888345637HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2386-2023·2023-08-23

    MAHURKAR dialysis catheters recalled for center lumen occlusion risk

    Covidien LP recalls MAHURKAR dialysis catheters due to excessive silicone lubricant on the catheter tip, which can obstruct the center lumen. This may delay treatment and cause serious blood complications including embolism and thrombosis.

    Product
    MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 16 cm, Curved Extensions, Kit" REF: 8888345611
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2408-2023·2023-08-23

    Infinity FMS Pak surgical device recalled for plastic debris hazard

    Alcon is recalling the Infinity FMS Pak surgical device after reports of patient injuries during procedures caused by plastic debris from over-tightening the included wrench. The recall affects 51,054 units distributed worldwide.

    Product
    Infinity FMS Pak
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2377-2023·2023-08-23

    Acute Dialysis Catheters Recalled for Catheter Tip Occlusion

    Covidien recalls 519 MAHURKAR acute dialysis catheters (Lot 2200400292) due to excessive silicone lubricant coating the catheter tip that may cause partial or full occlusion and treatment delays.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, PASS Tray REF: 8888104004HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2406-2023·2023-08-23

    Alcon Constellation Procedure Pak recalled due to plastic debris risk

    Alcon is recalling the Constellation Procedure Pak due to reports of patient injury from plastic debris. The debris can result from over-tightening the device with the included plastic wrench.

    Product
    Constellation Procedure Pak
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2374-2023·2023-08-23

    Dialysis Catheter Recall: Center Lumen Occlusion Due to Excessive Lubricant

    Covidien LP is recalling MAHURKAR 12 Fr dialysis catheters due to center lumen occlusion from excessive lubricant. The defect may cause treatment delays and serious complications including embolism and thrombosis.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, PASS Tray REF: 8888103002HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2373-2023·2023-08-23

    Dialysis Catheter Recall Due to Potential Lumen Occlusion

    Covidien LP is recalling MAHURKAR dialysis catheters due to excess silicone lubricant that can block the central lumen, potentially delaying treatment or causing serious complications.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, PASS Tray REF: 8888103001HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2390-2023·2023-08-23

    Dialysis Catheter Occlusion Recall Due to Excessive Lubricant Coating

    Covidien recalls 647 MAHURKAR dialysis catheters due to center lumen occlusion caused by excessive silicone lubricant. The blockage may delay treatment or increase risks of blood clots.

    Product
    MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 24 cm, Curved Extensions, Kit REF: 8888345637
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2389-2023·2023-08-23

    MAHURKAR Dialysis Catheter Recalled for Center Lumen Obstruction Risk

    Covidien LP recalled 15,209 MAHURKAR dialysis catheters due to excessive lubricant in the center lumen, which may cause catheter occlusion, reduce blood flow, or lead to hemolysis and blood clots.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, Kit REF: 8888345629HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2372-2023·2023-08-23

    FDA Recalls MAHURKAR Dialysis Catheters Over Obstruction Defect Risk

    Covidien's MAHURKAR dialysis catheters are recalled due to excessive lubricant on the catheter tip causing partial or complete obstruction. This risks delaying treatment and may cause blood clots, hemolysis, or embolism.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, IC Tray REF: 8888102004HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2371-2023·2023-08-23

    Dialysis Catheters Recalled for Catheter Obstruction from Excessive Silicone Lubricant

    Covidien is recalling 1,875 MAHURKAR dialysis catheters with lot numbers 2204000239 and 2227800110 due to excessive silicone lubricant causing catheter obstruction. The obstruction may delay treatment or cause hemolysis and thrombosis.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Straight Extensions, IC Tray REF: 8888102003HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2370-2023·2023-08-23

    Dialysis catheter recalled due to potential tip occlusion risk

    Covidien is recalling MAHURKAR dialysis catheters that may have excessive lubricant in the catheter tip, potentially causing obstruction. This could delay treatment or cause serious blood complications including thrombosis or embolism.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Curved Extensions, IC Tray REF: 8888101004HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2376-2023·2023-08-23

    Mahurkar Dialysis Catheters Recalled for Center Lumen Obstruction

    Covidien is recalling 1,099 MAHURKAR dialysis catheters worldwide due to excessive silicone lubricant that can block the center lumen, potentially delaying treatment.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Straight Extensions, PASS Tray REF: 8888104003HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2381-2023·2023-08-23

    MAHURKAR Dialysis Catheter Recalled for Excessive Lubricant Causing Occlusion

    The MAHURKAR dialysis catheter is recalled because excessive silicone lubricant can obstruct the center lumen, potentially delaying critical dialysis treatment.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, Kit REF: 8888340637HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2387-2023·2023-08-23

    Dialysis Catheters Recalled by FDA for Tip Obstruction Risk

    Covidien is recalling MAHURKAR acute dialysis catheters because the center lumen tip may be occluded by excessive silicone-based lubricant. Obstruction could delay treatment or cause embolism and thrombosis.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 16 cm, Curved Extensions, Kit REF: 8888345611HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2411-2023·2023-08-23

    Alcon Custom Pak Intraocular Lens Packages Recalled for Plastic Debris Risk

    Alcon Custom Pak intraocular lens packages are recalled due to reports of patient injury during surgical procedures caused by plastic debris from over-tightening with the included plastic wrench.

    Product
    Alcon Custom Pak
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1403-2023·2023-08-23

    Heinen's Cashew Butter Recalled for Undeclared Peanut and Almond

    Heinen's Fresh Ground Cashew Butter may contain undeclared peanut butter and/or almond butter. People with peanut or tree nut allergies could experience serious allergic reactions.

    Product
    Heinen's Fresh Ground Cashew Butter: packaged in plastic circle containers 1lb. Sold individually.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2367-2023·2023-08-23

    Covidien MAHURKAR Dialysis Catheter Recalled for Lumen Occlusion Risk

    Covidien is recalling dialysis catheters with excessive lubricant in the center lumen, which may cause occlusion, obstruct blood flow, and delay treatment.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, IC Tray REF:8888101001HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2379-2023·2023-08-23

    Dialysis Catheters Recalled Due to Excessive Lubricant Causing Obstruction

    Covidien is recalling MAHURKAR dialysis catheters that may have excessive lubricant coating the catheter tip, potentially causing dangerous blockages that delay treatment or lead to serious complications.

    Product
    MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Straight Extensions, Kit REF: 8888340629HP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2410-2023·2023-08-23

    Phaco Standalone Tips Recalled Due to Plastic Debris Risk

    Alcon is recalling 444,372 units of Phaco Standalone Tips worldwide because the plastic wrench included with the product can generate plastic debris when over-tightened, potentially injuring patients.

    Product
    Phaco Standalone Tips
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1437-2023·2023-08-23

    Pumpkin Creme Cookies Recalled Due to Undeclared Peanut Allergen

    Commercial Bakeries is recalling Ruxton Chocolates Manning Brand Pumpkin Creme Cookies because the product contains undeclared peanut. The recall affects 4834 cases distributed to retail locations in IL, NJ, MD, NY, CT, CA, and FL.

    Product
    Ruxton Chocolates Manning Brand Pumpkin Creme Cookies 19.5 oz. Bulk product packaged in bags, 12 bags per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1426-2023·2023-08-23

    Romaine Lettuce Mix Recalled for Potential Deer Feces Contamination

    G.O. Corporation is recalling lettuce mix containing romaine (Produce Code 421009) due to potential contamination with deer feces. The affected products were distributed in Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Lettuce Mix w 20 Romaine, Produce Code 421009, 4-5 lb. bags per shipping case,
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2421-2023·2023-08-23

    Surgical Clamp Recall: Rotation Knob May Crack or Break

    Snowden-Pencer endoscopic surgical clamps may have rotation knobs that crack or break due to manufacturing defect. Lot B23 units should not be used.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 50 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7045; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2419-2023·2023-08-23

    Surgical clamp rotation knob may crack or break due to manufacturing defect

    Specific lots of Snowden-Pencer surgical clamps may have rotation knobs that crack or break due to incorrect adhesive use in manufacturing. Eight units with lot numbers L22, B23, or C23 distributed in the US and Canada are affected.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH CLAMP DEBAKEY 25 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7043; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2426-2023·2023-08-23

    Endoscopic surgical graspers recalled for potential rotation knob failure

    Carefusion is recalling specific lots of Snowden-Pencer surgical graspers used in endoscopy due to a manufacturing defect that could cause the rotation knob to crack or break. The affected instrument may malfunction during surgical procedures.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH ATRAUMATIC GRASPER DIAMOND JAW 5MM, 45CM, RATCHETED, REF SP90-7220; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1431-2023·2023-08-23

    NatureBest Pre-Cut Lettuce Kits Recalled for Potential Deer Fecal Contamination

    NatureBest Pre-Cut & Produce LLC is recalling salad kits sold in Texas due to potential presence of deer fecal matter. No illnesses have been reported.

    Product
    SALAD KIT-NO COLOR-11CT LETTUCE-4 WAY/MIX-4/5# LETTUCE-ROM/GRN LF 60/40-4/3# LETTUCE-ROMAINE-SHREDDED-4/5# LETTUCE-ROM-1x1-GRN ONLY-6/2# LETTUCE-4 WAY/MIX-2/5# LETTUCE-4 WAY/MIX-1/5# LETTUCE-ROMAINE-CUT-6/2#
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1442-2023·2023-08-23

    Uro Kid Support Capsules recalled due to potential E. coli contamination

    Global Vitality Inc. is recalling Uro Kid Support Capsules due to potential E. coli contamination. The affected product was distributed to a single location in California.

    Product
    Food Research International - Uro Kid Support Capsules, packaged in glass bottle, 90 capsules per bottle, 12 bottles per case
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1414-2023·2023-08-23

    Dilettante Mocha Cafe Rheingold Dark Bulk Toffees recalled for incomplete allergen labeling

    Dilettante Chocolates Inc recalled Rheingold Dark Bulk Toffees distributed to Washington retail locations because the display placard's allergen declaration is incomplete. The placard states "Contains Dairy, Nuts" but does not specify the milk, almonds, and pecans present in the product.

    Product
    Dilettante Mocha Cafe brand Rheingold Dark Bulk Toffees, perishable, sold individual pieces out of retail display cases. The display placard declares butter, pecans, and almonds in the ingredients statement, but the Contains statement declares "Contains: Dairy, Nuts". Bulk truf
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·23V592000·2023-08-23

    Bentley Recalls 2017-2023 Bentayga Vehicles for Fuel Leak Fire Risk

    Bentley is recalling 2017-2023 Bentayga vehicles because fuel supply module wiring can overheat, melt a flange, and cause a fuel leak that increases fire risk.

    Product
    BENTLEY — BENTLEY BENTAYGA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2417-2023·2023-08-23

    Endoscopic surgical graspers recalled for potential rotation knob cracking

    Carefusion is recalling Snowden-Pencer MIS surgical graspers (lot B23) distributed in the US and Canada because the rotation knob may crack or break due to a manufacturing adhesive defect. Affected devices could malfunction during surgical use.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH ATRAUMATIC GRASPER DIAMOND JAW 5MM, 32CM, RATCHETED, REF SP90-7020; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·23V593000·2023-08-23

    Volkswagen Recalls 2024 Atlas Cross Sport for Engine Bearing Defect

    Volkswagen is recalling 2024 Atlas and Atlas Cross Sport vehicles because engine bearings may fail, causing engine stalls and increasing the risk of crashes and fires.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2429-2023·2023-08-23

    Snowden-Pencer Surgical Dissector Rotation Knob May Crack or Break

    Carefusion 2200 Inc is recalling specific lots of the Snowden-Pencer MIS surgical dissector because the rotation knob may crack or break due to a manufacturing defect.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR DIAMOND JAW 5MM, 45CM, RATCHETED, REF SP90-7271; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2401-2023·2023-08-23

    UroPass Ureteral Access Sheaths Recalled for Dilator Tip Breakage

    Olympus is recalling UroPass Ureteral Access Sheaths because dilator tips may break during surgical procedures or while in the package. The recall affects 9,520 units manufactured in 2018 and 2019.

    Product
    UroPass Ureteral Access Sheaths, 5 pieces/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1425-2023·2023-08-23

    Romaine lettuce blend recalled for potential fecal contamination

    G.O. Corporation is recalling a lettuce blend product due to potential contamination with deer feces. Affected products were distributed in Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Lett. Blend Rom/End/Rad-All Seasons packaged in the following sizes and configurations: 1. Produce Code 444032, 6-2 lb. bags per shipping case 2. Produce Code 444047, 3-2lb. bags per shipping case.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2424-2023·2023-08-23

    Endoscopic surgical grasper recalled due to rotation knob defect

    Carefusion is recalling specific lots of Snowden-Pencer Diamond-Touch endoscopic graspers due to a manufacturing defect that may cause the rotation knob to crack or break. Affected units were distributed in the US and Canada.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH GRASPERS CROCODILE GRASPER, DOUBLE ACTI 5MM, 32CM, RATCHETED HANDLE, REF SP90-7066; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2416-2023·2023-08-23

    Endoscopic Grasper Instrument Recalled for Rotation Knob Failure Risk

    Carefusion 2200 Inc is recalling specific lots of the Snowden-Pencer DIAMOND-TOUCH GRASPER endoscopic surgical instrument due to a manufacturing defect that may cause the rotation knob to crack or break, potentially compromising surgical performance.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH GRASPER DIAMOND JAW BABCOCK 5MM, 32CM, RATCHETED, REF SP90-7018; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2414-2023·2023-08-23

    FreeStyle Libre 2 Readers may fail to activate new sensors

    FreeStyle Libre 2 Readers may display an 'Incompatible Sensor' error when attempting to activate a new sensor after incomplete 14-day wear, potentially preventing new sensor activation and causing delayed glucose monitoring.

    Product
    FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2427-2023·2023-08-23

    Endoscopic surgical clamp recalled for potential rotation knob failure

    Carefusion recalls Snowden-Pencer MIS Diamond-Touch Clamps (Lot B23) due to potential cracking of the rotation knob from incorrect adhesive use. The 7 affected units were distributed to the US and Canada.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH CLAMP DEBAKEY 25 MM JAW 5MM, 45CM, RATCHETED, REF SP90-7243; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2423-2023·2023-08-23

    Surgical grasper recalled for rotation knob cracking due to adhesive defect

    Carefusion is recalling Snowden-Pencer endoscopic graspers due to potential rotation knob cracking from a manufacturing adhesive defect. Affected lot B23 was distributed in the US and Canada.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH GRASPER CRILE CURVED JAW 5MM, 32CM, RATCHETED, REF SP90-7048; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2422-2023·2023-08-23

    Endoscopic Surgical Clamp Recalled Due to Potential Rotation Knob Failure

    Carefusion is recalling specific lots of Snowden-Pencer MIS endoscopic surgical clamps due to potential cracking or breaking of the rotation knob caused by incorrect adhesive use during manufacturing.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH CLAMP BOWEL 60 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7046; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2415-2023·2023-08-23

    Snowden-Pencer Surgical Grasper Recalled for Cracking Rotation Knob

    Carefusion 2200 Inc is recalling specific lots of the Snowden-Pencer MIS Diamond-Touch Grasper surgical tool due to defects in the rotation knob adhesive that may cause cracking or breaking during use.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH GRASPER MCKERNAN FUNDUS 5MM, 32CM, RATCHETED, REF SP90-7012; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2418-2023·2023-08-23

    Endoscopic Dissector Surgical Tool Recalled for Cracking Knob Defect

    Carefusion 2200 Inc is recalling Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR endoscopic surgical instruments due to potential cracking of the rotation knob from incorrect adhesive use in manufacturing. Lot B23 is affected.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR FENESTRATED 16MM JAW 5MM, 32CM, NON RATCHETED, REF SP90-7036; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2428-2023·2023-08-23

    Endoscopic Surgical Grasper Recalled for Potential Rotation Knob Cracking

    Carefusion is recalling specific lots of surgical graspers due to potential cracking of the rotation knob caused by incorrect adhesive use in manufacturing. Affected devices may fail during surgical procedures.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH GRASPERS CROCODILE GRASPER, DOUBLE ACTI 5MM, 45CM, RATCHETED HANDLE, REF SP90-7266; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2420-2023·2023-08-23

    Endoscopic surgical clamp recalled for defective rotation knob

    Carefusion 2200 Inc is recalling specific lots of Snowden-Pencer MIS DIAMOND-TOUCH surgical clamps because the rotation knob may crack or break due to a manufacturing defect. Lots B23 and C23 are affected.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH CLAMP DEBAKEY 35 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7044; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2405-2023·2023-08-23

    Hip Screw Labeled as Wrong Size: 30mm Screws Mislabeled as 25mm

    Conformis hip screws measuring 30mm have been mislabeled as 25mm, creating risk of incorrect surgical implantation. The recall affects 25 units distributed across nine states.

    Product
    CONFORMIS HIP-SCREW-6.5MM X 25MM, STERILE EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2407-2023·2023-08-23

    Centurion FMS Pak Recalled Due to Patient Injury Risk from Plastic Debris

    Alcon Research recalls the Centurion FMS Pak following reports of patient injury during procedures. Plastic debris can result from over-tightening with the included plastic wrench.

    Product
    Centurion FMS Pak
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1428-2023·2023-08-23

    Lettuce Rom Blend recalled due to potential deer feces contamination

    G.O. Corporation is recalling Lettuce Rom Blend (23,186 lbs.) distributed to IA, MN, ND, and WI because the lettuce may be contaminated with deer feces.

    Product
    Lettuce Rom Blend 50/50, packaged in the following sizes and configurations: 1. Produce Code 448909, 4-5 lb. bags per shipping case, Customer UPC 3127222; 2. Produce Code 449007, 2-5 lb. bags per shipping case, Customer UPC 6862312; 3. Produce Code 449009, 4-5 lb. b
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1429-2023·2023-08-23

    Romaine Lettuce Recalled Due to Potential Deer Feces Contamination

    G.O. Corporation is recalling Romaine Lettuce All American sold in four states due to potential contamination with deer feces.

    Product
    Lettuce Romaine All American, packaged in the following sizes and configurations: 1. Produce Code 476702, 1-5 lb. bag per shipping case, Customer UPC 8398299; 2. Produce Code 476709, 4-5 lb. bags per shipping case, Customer UPC 476709, 8336156, and 8398281.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1430-2023·2023-08-23

    Lettuce Salad Mix Recalled for Potential Deer Feces Contamination

    G.O. Corporation is recalling Lettuce Salad Shred Mix due to potential contamination with deer feces. The affected products were distributed in Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Lett. Salad Shred Mix w/Rom, Produce Code 458009, 4-5 lb. bags per shipping case, Customer UPC 7561965.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1438-2023·2023-08-23

    Trader Joe's Gluten-Free Joe-Joe's Cookies Recalled for Undeclared Peanut

    Trader Joe's Gluten Free Joe-Joe's Chocolate Vanilla Creme Sandwich Cookies are being recalled due to undeclared peanuts. The recalled product was distributed to stores in seven states.

    Product
    Trader Joe's Gluten Free Joe-Joe's Chocolate Vanilla Creme Sandwich Cookies Net Wt.12.5 oz (354g) UPC: 0050 7547 Packaged in paper cartons. 25 retail units per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1416-2023·2023-08-23

    Dilettante Mocha Cafe Toffee Recalled for Incomplete Allergen Labeling

    Dilettante Chocolates recalls Rheingold White Bulk Toffee sold at Washington retail locations due to display placard with incomplete allergen declarations. The placard did not fully identify milk and specific nut allergens present in the product.

    Product
    Dilettante Mocha Cafe brand Rheingold White Bulk Toffee, perishable, sold individual pieces out of retail display cases. The display placard declares milk, pecans and hazelnuts in the first Contains statement, and the 2nd Contains statement declares "Contains: Dairy, Nuts". Bu
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1424-2023·2023-08-23

    Lettuce Salad Blend Monterey recalled due to potential deer feces contamination

    G.O. Corporation is recalling Lettuce Salad Blend Monterey (Produce Code 404709) from Iowa, Minnesota, North Dakota, and Wisconsin due to potential contamination with deer feces. The recall affects 23,186 pounds across lot codes 130209 and 130212.

    Product
    Lettuce Salad Blend Monterey, Produce Code 404709, 4-5lb. bags per shipping case.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1434-2023·2023-08-23

    Benton's Snack Packs Recalled for Undeclared Peanut Allergen

    Benton's 100 Calorie Snack Packs are recalled because they contain undeclared peanut, a major allergen. Consumers with peanut allergies may experience severe reactions if they consume this product.

    Product
    Benton's 100 Calorie Snack Packs Baked Chocolate Wafer Snacks 6-0.81 OZ (23g) Packs Net Wt. 4.86 oz UPC: 4 099100 040416 Packaged in a paper carton, 16 cartons per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1443-2023·2023-08-23

    Brain Enhancer Capsules Recalled for Potential E. coli Contamination

    Global Vitality Inc. is recalling Food Research International Serious Brain Enhancer Capsules due to potential E. coli contamination. The product was distributed to a single location in California.

    Product
    Food Research International - Serious Brain Enhancer Capsules, packaged in glass bottle, 90 capsules per bottle, 12 bottles per case
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1408-2023·2023-08-23

    Dilettante Mocha Cafe Champagne Truffles recalled for milk allergen labeling discrepancy

    Dilettante Mocha Cafe Champagne Bulk Truffles are being recalled due to milk allergen labeling errors on display case placards in Washington. The allergen declaration does not adequately reflect milk content.

    Product
    Dilettante Mocha Cafe brand Champagne Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail stores c
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1432-2023·2023-08-23

    Garden Cut Romaine Lettuce Recalled for Potential Deer Feces Contamination

    Get Fresh Produce is recalling Garden Cut Romaine lettuce (product 9386) because it may be contaminated with deer feces. The recall affects 1,404 pounds distributed in Illinois and Florida.

    Product
    Garden Cut Romaine 1x1 Chopped 6/2 LB (product number 9386) packed in corrugated boxes with an inner plastic bag (6, 2lb bags per case)
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1423-2023·2023-08-23

    Romaine lettuce recalled due to potential deer feces contamination

    G.O. Corporation is recalling romaine lettuce in multiple package sizes due to potential contamination with deer feces. The affected products were distributed to Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Romaine lettuce packaged into the following configurations and sizes: 1. Lettuce Romaine Shred, Produce Code 720325, 4-2.5lb. bags per shipping case, Customer UPC 9120457. 2. Romaine Shred 1/4", Produce Code 720425, 4-2.5lb bags per shipping case, Customer UPC 7641269 and
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1441-2023·2023-08-23

    Ginger Snap Cookies Recalled for Undeclared Peanut Allergen

    Simply MI-Delicious Swedish Style Ginger Snaps are recalled due to undeclared peanut. People with peanut allergies are at risk.

    Product
    Simply MI-Delicious MI-DEL Swedish Style Ginger Snaps Net Wt. 10 oz (284g)UPC:3068403502. Packaged in plastic bags, 12 bags per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1440-2023·2023-08-23

    Trader Joe's Joe-Joe's Cookies Recalled for Undeclared Peanut Allergen

    Commercial Bakeries is recalling Trader Joe's Joe-Joe's Chocolate Vanilla Creme cookies due to undeclared peanut allergen. Consumers with peanut allergies should not consume this product and should return it to the store.

    Product
    Trader Joe's Joe-Joe's Chocolate Vanilla Creme Flavored With Other Natural Flavors Net Wt.13.4 oz (380g) UPC: 0076 5725 Packaged in trays. 26 units per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1427-2023·2023-08-23

    Romaine Lettuce Recalled Due to Deer Feces Contamination

    G.O. Corporation is recalling Romaine Lettuce 80/20 GB due to potential contamination with deer feces. The affected products were distributed to Iowa, Minnesota, North Dakota, and Wisconsin.

    Product
    Lettuce Romaine 80/20 GB, packaged in the following sizes and configurations: 1. Produce Code 448007, 2-5 lb. bags per shipping case, 2. Produce Code 448007, 4-5 lb. bags per shipping case, 3. Produce Code 448110, 4-5 lb. bags per shipping case.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1410-2023·2023-08-23

    Dilettante Mocha Cafe Amaretto Bulk Truffle Allergen Labeling Error

    Dilettante Chocolates is recalling Mocha Cafe brand Amaretto Bulk Truffle chocolate sold from retail display cases due to incomplete allergen declaration on the display placard.

    Product
    Dilettante Mocha Cafe brand Amaretto Bulk Truffle, perishable, sold individual pieces out of retail display cases. The display placard declares milk chocolate and almond extract in the ingredients statement, but the Contains statement declares "Contains: Dairy, Nuts". Bulk truf
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1435-2023·2023-08-23

    Annie's Homegrown Graham Snack Recalled for Undeclared Peanut

    Annie's Homegrown Gluten Free Bunny Grahams Cocoa & Vanilla 6.75 oz boxes are recalled due to undeclared peanut. Consumers with peanut allergies should not consume this product.

    Product
    Annie's Homegrown Gluten Free Bunny Grahams Cocoa & Vanilla Flavored With Other Natural Flavors Graham-Style Snacks Net Wt 6.75 oz (191g) UPC: 13562 00019 Packaged in cartons, 7 and 12 retails cartons per case
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1405-2023·2023-08-23

    Dilettante Dark Ephemere Bulk Truffles Milk Allergen Mislabeling

    Dilettante Mocha Cafe Dark Ephemere Bulk Truffles' display placard lists milk in ingredients but declares only 'Contains: Dairy,' not 'Contains: Milk.' Bulk boxes have correct allergen labeling.

    Product
    Dilettante Mocha Cafe brand Dark Ephemere Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk, cream, and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1433-2023·2023-08-23

    Garden Cut Lettuce Greek Mix Salad recalled for possible deer feces contamination

    Get Fresh Produce, Inc. is recalling Garden Cut Lettuce Greek Mix Salad (product number 10149) due to possible contamination with deer feces. Affected product was distributed in Illinois and Florida.

    Product
    Garden Cut Lettuce Greek Mix Salad (product number 10149) 10 LB packed in corrugated boxes with an inner plastic bag. Product consists of: 1"x1" Romaine, 1/8" red cabbage, and 1/8" green cabbage.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1402-2023·2023-08-23

    Trader Joe's Falafel Recalled for Foreign Object Contamination

    Trader Joe's Fully Cooked Falafel Heat & Eat is being recalled from Connecticut, Texas, and Illinois due to the presence of rocks in the product. Consumers should return affected packages to the point of purchase.

    Product
    Trader Joe's Fully Cooked Falafel Heat & Eat NET WT. 12 OZ (340g) Distributed and Sold Exclusively By: Trader Joe's Monrovia, CA 91016 UPC 0093 9355
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1406-2023·2023-08-23

    Dilettante Mocha Cafe Truffles recalled for incomplete milk allergen labeling

    Dilettante Chocolates Inc is recalling Mocha Cafe brand Light Ephemere Bulk Truffles sold from retail display cases in Washington due to incomplete allergen labeling on the display placard.

    Product
    Dilettante Mocha Cafe brand Light Ephemere Bulk Truffles, perishable, sold in individual pieces out of retail display cases. The display placard declares cream and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1459-2023·2023-08-23

    IO Inspired Organics Walnut Halves & Pieces recalled for undeclared walnuts

    IO Inspired Organics Walnut Halves & Pieces are recalled because walnuts are not declared in the ingredient and contains statement. The 7oz packages were distributed in 11 states and may pose a risk to consumers with walnut allergies.

    Product
    IO Inspired Organics brand Organic Raw Walnut Halves & Pieces; 7oz plastic tubs; 9 packages per wholesale case; retail UPC 863669740065, Lipari #943469
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-1436-2023·2023-08-23

    Gluten Free MI-DEL Swedish Style Ginger Snaps recalled for undeclared peanut

    Gluten Free MI-DEL Swedish Style Ginger Snaps (8 oz and 10 oz packages) are being recalled because they contain undeclared peanut. Consumers with peanut allergies should not consume this product and should return it to the retailer or dispose of it safely.

    Product
    Gluten Free MI-DEL Swedish Style Ginger Snaps Net Wt. 8 oz (227g) & 10 oz UPC:3068476890. Packaged in plastic bags, 12 bags per case.
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-2413-2023·2023-08-23

    HF Resection Electrodes Recalled for Wire Breakage and Patient Fragment Hazard

    Olympus HF Resection Electrodes are being recalled due to reports of loop wire breakage when contacting metal objects. Broken fragments can fall inside the patient and require retrieval.

    Product
    HF Resection Electrodes - HF resection electrodes are part of a resectoscope system for endoscopic diagnosis and treatment in urological or gynecological applications. 64 Models: 1) A22201C 2) A22201D 3) A22202C 4) A22203C 5) A22205C 6) A22205D 7) A22206C 8) A2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1084-2023·2023-08-23

    Toothpaste Label Mix-Up: Wrong Tube Labels in Strawberry Cartons

    Hello wild strawberry fluoride toothpaste cartons contain tubes incorrectly labeled as hello fresh watermelon fluoride free toothpaste. 182,046 units affected nationwide.

    Product
    hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% (0.15% w/v fluoride ion), NET WT 4.2 OZ (119 g), Distributed by Hello Products LLC, Montclair, NJ 07042, UPC 8 19156 02026 4 (carton), 12-count case GTIN: 20819156020268; strawberry tubes also sold in Strawberry 3-p
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2425-2023·2023-08-23

    Endoscopic Surgical Dissectors Recalled for Potential Rotation Knob Cracking

    Carefusion 2200 Inc recalls 42 units of Snowden-Pencer surgical dissectors distributed in the US and Canada due to potential cracking of the rotation knob caused by an adhesive defect in manufacturing.

    Product
    Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR DIAMOND JAW 5MM, 32CM, RATCHETED, REF SP90-7071; endoscopic surgical device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1448-2023·2023-08-23

    Frozen Sachertote Recalled for Undeclared Egg, Milk, and Wheat Allergens

    Lidl US TRADING is recalling Alpenfest Style Sachertote frozen dessert because egg, milk, and wheat allergens are not declared on the label. Consumers with allergies to these ingredients should not consume the product.

    Product
    Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen UPC:2010 0889 Packaged in Cardboard Carton.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-2412-2023·2023-08-23

    Medtronic ventricular catheter system recalled due to incorrect labeling expiration date

    Medtronic is recalling 44 units of the Duet External Drainage and Monitoring system because the product labels contain an incorrect expiration date. The affected lot (226632942) was distributed nationwide.

    Product
    Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1085-2023·2023-08-23

    PLUVICTO Injection Recalled for Incorrect Lot and Expiration Date Labels

    PLUVICTO (lutetium Lu 177 vipivotide tetraxetan) injection vials were labeled with incorrect lot numbers and expiration dates. The manufacturer is recalling affected lots distributed nationwide.

    Product
    PLUVICTO 1,000MBq/mL (27 mCi/mL), lutetium Lu 177 vipivotide tetraxetan injection, 9.2 mL Single-dose vial, Manufacturer: Advanced Accelerator Appllications USA, Inc., 57 E. Willow Street NJ 07041, Milburn, USA, NDC 69488-010-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1417-2023·2023-08-23

    Dilettante Mocha Cafe Sriracha Bulk Caramels Recalled for Labeling Inconsistency

    Dilettante Chocolates is recalling Mocha Cafe brand Sriracha Bulk Caramels sold at Washington retail locations due to inconsistent dairy allergen labeling on display case placards versus case boxes.

    Product
    Dilettante Mocha Cafe brand Sriracha Bulk Caramels, perishable, sold individual pieces out of retail display cases. The display placard declares cream and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to reta
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1411-2023·2023-08-23

    Dilettante Dark Ginger Bulk Truffles Recalled for Inadequate Milk Allergen Labeling

    Dilettante Chocolates recalled Dark Ginger Bulk Truffles from Washington retail stores because the display placard's allergen declaration fails to clearly identify milk. The product boxes have the correct label.

    Product
    Dilettante Mocha Cafe brand Dark Ginger Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail stores
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1447-2023·2023-08-23

    Newly Weds Foods Curing Salt Recalled Due to Metal Contamination

    Newly Weds Foods, Inc. is recalling its G25928 Curing Salt product because it may contain small pieces of metal. Affected consumers should not use this product.

    Product
    Newly Weds Foods G25928 CURE 6.25% W/SALT W/O ADDITIVES X1 50lbs
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-1418-2023·2023-08-23

    Dilettante Mocha Cafe Espresso Bulk Caramels Recalled for Labeling Discrepancy

    Dilettante Chocolates is recalling Mocha Cafe Espresso Bulk Caramels sold at its Washington retail locations due to a display placard allergen declaration that states 'Contains: Dairy' instead of 'Contains: Milk,' though milk is listed in the ingredients.

    Product
    Dilettante Mocha Cafe brand Espresso Bulk Caramels, perishable, sold individual pieces out of retail display cases. The display placard declares milk in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail stores co
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1419-2023·2023-08-23

    Dilettante Mocha Cafe Caramels Display Placard Allergen Labeling Inconsistency

    Dilettante Chocolates Inc is recalling caramels sold from display cases because the display placard's allergen statement is incomplete. The placard lists only 'Contains: Dairy' despite cream and butter being shown in the ingredients list.

    Product
    Dilettante Mocha Cafe brand Himalayan Pink Salt Bulk Caramels, perishable, sold individual pieces out of retail display cases. The display placard declares cream and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes s
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1412-2023·2023-08-23

    Dilettante Mocha Cafe Praline Truffles Recalled for Imprecise Allergen Labeling

    Dilettante Chocolates Inc recalled Dilettante Mocha Cafe brand Praline Bulk Truffles because display placards use general allergen categories (Dairy, Nuts) instead of specific allergen sources (Milk, Almond, Pecan).

    Product
    Dilettante Mocha Cafe brand Praline Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk, pecans, and almonds in the ingredients statement, but the Contains statement declares "Contains: Dairy, Nuts". Bulk truffle boxe
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1413-2023·2023-08-23

    Dilettante Espresso Truffles Recall: Incomplete Allergen Labeling on Display

    Dilettante Chocolates recalls Mocha Cafe Espresso Bulk Truffles sold at Washington retail locations. The retail display placard's allergen statement declares 'Contains: Dairy' instead of the required 'Contains: Milk.'

    Product
    Dilettante Mocha Cafe brand Espresso Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail stores co
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1086-2023·2023-08-23

    Tobramycin Ophthalmic Solution recalled for failed quality specifications

    Alembic Pharmaceuticals is recalling 82,400 bottles of Tobramycin Ophthalmic Solution nationwide because the product failed to meet impurities and degradation specifications.

    Product
    TOBRAMYCIN OPHTHALMIC SOLUTION — TOBRAMYCIN OPHTHALMIC SOLUTION (TOBRAMYCIN OPHTHALMIC SOLUTION)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1407-2023·2023-08-23

    Dilettante Mocha Cafe Dark Raspberry Truffles display placard mislabeled for allergens

    Dilettante Chocolates recalls Mocha Cafe Dark Raspberry Bulk Truffles sold at retail stores in Washington due to incomplete allergen labeling on display placards. The product contains dairy but the allergen declaration is incomplete.

    Product
    Dilettante Mocha Cafe brand Dark Raspberry Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares cream and butter in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent t
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1445-2023·2023-08-23

    Bacon Cure Product Recalled for Possible Metal Contamination

    Newly Weds Foods recalls a bacon cure product due to possible contamination with small metal pieces. Consumers who purchased this product should not use it.

    Product
    Newly Weds Foods R03361 HAHN'S SPECIAL BACON CURE HS X1 40lbs
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-1420-2023·2023-08-23

    Dilettante Mocha Cafe Alderwood Smoked Caramels Display Label Milk Allergen Inconsistency

    Retail display placard for Dilettante Mocha Cafe Alderwood Smoked Bulk Caramels sold in Washington contains inconsistent milk allergen labeling: milk is listed in ingredients but the Contains statement says 'Dairy' instead of 'Milk.'

    Product
    Dilettante Mocha Cafe brand Alderwood Smoked Bulk Caramels, perishable, sold individual pieces out of retail display cases. The display placard declares milk in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail s
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1444-2023·2023-08-23

    Pork Roll Cure Recalled for Potential Small Metal Contamination

    Newly Weds Foods is recalling a pork roll cure product due to potential contamination with small metal pieces. Consumers who have this product should stop using it.

    Product
    Newly Weds Foods R03810 LOEFFLER COMP PORK ROLL CURE X1 54lbs
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-1415-2023·2023-08-23

    Dilettante Mocha Cafe Bulk Toffee Chocolates Incomplete Allergen Declaration Recall

    Dilettante Mocha Cafe brand Rheingold Milk Bulk Toffee chocolates are being recalled due to incomplete allergen information on retail display case placards. The placard states 'Contains: Dairy, Nuts' but does not specify which nuts (almonds and pecans) are present in the product.

    Product
    Dilettante Mocha Cafe brand Rheingold Milk Bulk Toffee, perishable, sold individual pieces out of retail display cases. The display placard declares milk, pecans, and almonds in the ingredients statement, but the Contains statement declares "Contains: Dairy, Nuts". Bulk truffle
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1439-2023·2023-08-23

    Trader Joe's Tiniest Chocolate Chip Cookies Recalled for Undeclared Peanut

    Commercial Bakeries is recalling Trader Joe's Tiniest Chocolate Chip Cookies due to undeclared peanut. Consumers with peanut allergies should not consume this product.

    Product
    Trader Joe's Tiniest Chocolate Chip Cookies Net Wt. 8 oz (227 g) UPC: 0076 3691 Packaged in bags. 24 bags per case.
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Food)·F-1409-2023·2023-08-23

    Dilettante Mocha Cafe Dark Chocolate Truffles Display Placard Allergen Labeling Error

    Dilettante Chocolates recalls display placards for L'Orange Dark Bulk Truffles due to incomplete allergen labeling. The placard's allergen warning does not clearly state milk, though the actual product packaging is correctly labeled.

    Product
    Dilettante Mocha Cafe brand L'Orange Dark Bulk Truffles, perishable, sold individual pieces out of retail display cases. The display placard declares milk in the ingredients statement, but the Contains statement declares "Contains: Dairy". Bulk truffle boxes sent to retail stor
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1422-2023·2023-08-23

    Zephyrhills Spring Water recalled due to bromate contamination

    Blue Triton is recalling certain batches of Zephyrhills 100% Natural Spring Water 16.9 FL Oz bottles distributed domestically due to bromate levels exceeding EPA maximum contaminant limits. Consumers should discontinue use of affected batches.

    Product
    1964 Zephyrhills 100% Natural Spring Water 16.9 FL Oz (500 mL)
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·23V591000·2023-08-22

    Harley-Davidson Softail Motorcycles Recalled for Faulty Shock Absorber Fastener

    Harley-Davidson is recalling certain 2018–2023 Softail motorcycles where a fastener securing the rear shock absorber may break, causing tire damage and loss of tire pressure. This can lead to loss of vehicle control and increased crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FXLRST, FXRST, FLHC, FLHCS ANV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E062000·2023-08-21

    Outfitter Truck Campers Recalled for Potential Gas Leak Fire Risk

    Outfitter is recalling 2021-2022 truck campers because aluminum burner tubes may fracture, causing a gas leak that could lead to fire.

    Product
    OUTFITTER MANUFACTURING — OUTFITTER MANUFACTURING CARIBOU LITE 6.5, CARIBOU LITE 8.5, APEX 8, CARIBOU 6.5
    Category
    Vehicle
    Distribution
    Distributed nationwide

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