The Recall Desk

Archive

February 2024 recalls

677 recalls were announced in February 2024.

What the numbers show

Critical
21
Severe
160
High
457
Moderate
38
Low
1

Of the 677 recalls this month scored against our rubric, 3% are Critical, 24% are Severe.

1–100 of 677

  • SevereNHTSA·24V165000·2024-02-29

    BMW motorcycle front struts can fail causing loss of stability

    BMW is recalling certain 2024 R 1250RT, K 1600GT, K 1600GTL and K 1600B motorcycles because an incorrectly manufactured proportional valve in the front spring strut can loosen and cause strut failure.

    Product
    BMW — BMW K 1600 GTL, K 1600 GT, K 1600 B, R 1250 RT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V163000·2024-02-29

    Land Rover Recalls 2024 Discovery Sport for A-Pillar Bolt Issue

    Land Rover is recalling 2024 Discovery Sport vehicles because a lower A-pillar bolt may be improperly fastened, reducing structural strength and increasing injury risk in a crash.

    Product
    LAND ROVER — LAND ROVER DISCOVERY SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·009-2024·2024-02-29

    MF Meats Recalls Raw Meat Products Contaminated with Non-Food Grade Oil

    MF Meats is recalling approximately 93,277 pounds of raw meat products that may be contaminated with non-food grade mineral seal oil. The products were shipped to restaurants in New York, Ohio, and Pennsylvania.

    Product
    MF Meats — MF Meats Recalls Raw Meat Products Due to Contamination by a Non-Food Grade Substance
    Category
    Food
    Distribution
    3 states
  • SevereCPSC·24137·2024-02-29

    Camplux Portable Tankless Water Heaters Recalled Due to Fire Hazard

    About 42,000 Camplux portable tankless water heaters can leak gas from the regulator connection, creating a fire hazard. The Home Appliances is offering free repair kits with replacement regulators.

    Product
    Camplux portable tankless water heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V164000·2024-02-29

    International truck steering gear teeth can crack causing steering loss

    Navistar is recalling certain 2025 International HV, HX, LT and MV vehicles because an improperly heat-treated steering gear sector shaft can crack or fracture, causing a loss of steering control.

    Product
    INTERNATIONAL — INTERNATIONAL HX, MV, HV, LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E020000·2024-02-29

    BMW Recalls R 1300 GS Dealer Accessory Top Cases

    BMW is recalling R 1300 GS dealer accessory top cases because the locking flap may fail, causing the case to detach and create a road hazard.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24135·2024-02-29

    Oso & Me Children's Pajama Sets Recalled for Flammability Hazard

    Oso & Me is recalling approximately 170 children's pajama sets that violate federal flammability regulations for sleepwear, posing a burn risk to children. No injuries have been reported.

    Product
    Children's Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V161000·2024-02-29

    Jayco Recalls 2023-2025 Entegra Motorhomes for Steering Gear Defect

    Jayco is recalling 2023-2025 Entegra Coach Anthem and Cornerstone motorhomes because foreign material in the steering gear may cause a loss of power steering assist.

    Product
    ENTEGRA — ENTEGRA ANTHEM, CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24138·2024-02-29

    Liverpool Football Club Children's Pajamas Recalled for Burn Hazard

    About 720 Liverpool Football Club children's pajamas fail to meet federal flammability standards for sleepwear, posing a burn-injury risk. The pajamas were sold exclusively online from January 2022 through November 2023.

    Product
    Liverpool Football Club (L.F.C.) Children's Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24140·2024-02-29

    Ski-Doo MXZ and Renegade Snowmobiles Recalled for Ski Breakage Risk

    BRP is recalling about 8,100 2024 Ski-Doo MXZ and Renegade snowmobiles equipped with Pilot X skis because the left ski can break, creating a risk of serious injury and crash. Consumers should stop using the snowmobiles immediately and contact BRP for a free ski replacement.

    Product
    Ski-Doo® MXZ and Renegade Snowmobiles equipped with Pilot X Skis
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24136·2024-02-29

    Cannondale Dave Bicycles Recalled for Fall and Injury Hazards

    Cannondale is recalling 2021–2023 Model Year Dave bicycles because the headtube/downtube weld can become damaged and separate from the frame, creating a fall hazard. No injuries have been reported.

    Product
    2021 through 2023 Model Year Cannondale Dave bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V160000·2024-02-29

    Motorhome battery relays can stick closed creating charging fire risk

    Jayco is recalling certain 2021-2024 Solstice LI, Swift, Terrain, Terrain LE, Ethos LI, Expanse LI and Launch LE motorhomes because battery relay contactors may become stuck closed.

    Product
    ENTEGRA — ENTEGRA, JAYCO LAUNCH, SOLSTICE LI, SWIFT, TERRAIN LE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24142·2024-02-29

    Heritage Store Hydrogen Peroxide Mouthwash Lacks Child-Resistant Packaging

    Nutraceutical Corporation is recalling Heritage Store Hydrogen Peroxide Mouthwash because the packaging does not comply with child-resistant packaging requirements, posing a poisoning risk if swallowed by young children.

    Product
    Heritage Store Hydrogen Peroxide Mouthwash
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24141·2024-02-29

    Sandford Family 6-Player Croquet Sets Recalled for Lead and Phthalates

    Sandford Family 6-Player Croquet Sets are recalled because paint on mallets, hoops, and winning posts contains lead and phthalates at levels that exceed federal bans. Lead and phthalates are toxic if ingested, especially for young children.

    Product
    Sandford Family 6-Player Croquet Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24133·2024-02-29

    Vanilla Underground Minecraft TNT Children's Pajamas Recalled for Burn Hazard

    About 1,570 Vanilla Underground "Minecraft TNT" one-piece pajamas fail to meet federal flammability regulations for children's sleepwear, posing a burn injury risk. Consumers should stop using them immediately and contact Vanilla Underground for a refund.

    Product
    Vanilla Underground "Minecraft TNT" One-Piece Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24134·2024-02-29

    Electric Height-Adjustable Mobile Stands for Displays Recalled for Tip-Over Hazard

    SMART Technologies is recalling about 750 electric height-adjustable mobile stands for large interactive flat panel displays because wheelbase welds can bend or break during movement, causing the stands to tip over and create entrapment hazards.

    Product
    Electric Height-Adjustable Mobile Stands for Large Interactive Flat Panel Displays
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24132·2024-02-29

    Vernier Go Direct Charge Stations Recalled Due to Burn Hazard

    Vernier Science Education is recalling about 15,000 Go Direct Charge Stations because they can overheat and pose a burn hazard. The company has received two reports of overheating but no injuries have been reported.

    Product
    Vernier Go Direct® Charge Stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1081-2024·2024-02-28

    Surgical ocular pack kits recalled due to saline sterility assurance loss

    Windstone Medical Packaging is recalling 80 Aligned Medical Solutions ocular pack surgical kits because sterility of the included saline cannot be guaranteed.

    Product
    Aligned Medical Solutions, In House Ocular Pack, AMS12947, STERILEEO
    Category
    Medical Device
    Distribution
    3 states
  • CriticalFDA (Devices)·Z-1046-2024·2024-02-28

    Dover Foley catheter kits recalled due to defective supplier components

    Cardinal Health is recalling Dover brand Foley catheter kits due to components recalled by supplier Nurse Assist. Approximately 435,060 units were distributed to the US, Europe, Japan, and Latin America.

    Product
    Dover URINE METER ADD-A-FOLEY TRAY, 200 ML, NEEDLE SAMPLING PORT, DRAIN TUBE, PREP TRAY; Dover UNIVERSAL TRAY, 1000 ML BASIN, PVP SWAB STICKS, PREPPING COMPONENTS, 30 CC PRE-FILLED SYRINGE; Dover URINE DRAINAGE ADD-A-FOLEY TRAY, NEEDLE SAMPLING, A/R, DRAIN TUBE, PREP TRAY, 30 ML
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1050-2024·2024-02-28

    Dover Foley Catheter Kits Recalled Due to Defective Components

    Cardinal Health is recalling 4,620 Dover Foley catheter convenience kits due to components that were recalled by Nurse Assist. The kits, distributed in the US, EMEA, Japan, and Latin America, contain silicone and latex catheters.

    Product
    Dover" 100% SILICONE FOLEY TRAY, LUER LOCK, 16 FR (5.3 MM), 5 CC, 2000 ML DRAIN BAG, DRAIN SPOUT; Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, LUER LOCK, 16 FR (5.3 MM), 5 CC, 2000 ML DRAIN BAG; Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, COUD¿ TIP, 16 FR (5.3 MM), 5 CC, 2000 ML D
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0343-2024·2024-02-28

    Herbal dietary supplement recalled for undeclared drug ingredient

    Sustain Herbal Dietary Supplement is being recalled nationwide for containing undeclared tadalafil, a pharmaceutical ingredient. The product was marketed as a dietary supplement but contains an unapproved drug.

    Product
    Sustain Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by VSD Productions, Inc. Las Vegas, Nevada
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0334-2024·2024-02-28

    Drug Recalled for Marketing Unapproved Tianeptine Without FDA Approval

    Neptune's Fix Tianeptine Elixir is recalled nationwide for containing tianeptine, an FDA-unapproved substance. The product was marketed without required FDA approval.

    Product
    Neptune's Fix, Tianeptine Extra Strength Elixir, 0.338 fl oz (10 mL) bottle, Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1052-2024·2024-02-28

    Dover Foley Catheter Kits and Drain Trays Recalled

    Dover Foley catheter kits and silicone drain trays manufactured with subsequently recalled components were distributed to 924 units across the US, EMEA, Japan, and Latin America.

    Product
    Dover" 100% SILICONE FOLEY TRAY, NEEDLELESS, 14 FR (4.7 MM), 5 CC, 2000 ML DRAIN BAG, DRAIN SPOUT; Dover" HYDROGEL COATED LATEX FOLEY CATHETER KIT, 5 CC, 2-WAY, 14 FR (4.7 MM), 10 CC WATER SYRINGE
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0909-2024·2024-02-28

    Hale and Hearty Tomato Basil and Rice Soup Recalled for Undeclared Soy

    Hale and Hearty Soups is recalling Tomato Basil and Rice soup (UPC 635508547872) due to undeclared soy allergen. Consumers with soy allergies should not consume this product.

    Product
    Hale and Hearty Soups; Tomato Basil and Rice; UPC 635508547872
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1080-2024·2024-02-28

    Surgical ocular packs recalled for loss of saline sterility

    Windstone Medical Packaging recalled 128 surgical eye kits because the included saline cannot be guaranteed sterile, risking post-operative infection.

    Product
    Aligned Medical Solutions, In House Ocular Pack, AMS12947A STERILEEO
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0344-2024·2024-02-28

    SCHWINNNG Herbal Dietary Supplement Recalled for Undeclared Nortadalafil Content

    SCHWINNNG Herbal Dietary Supplement (Lot #2108, exp. 10/31/2024) is recalled nationwide because it contains undeclared nortadalafil, an active pharmaceutical ingredient used for male sexual enhancement. The FDA classified this as an unapproved drug.

    Product
    SCHWINNNG Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Today the World LLC, Vancouver, WA 98683
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0345-2024·2024-02-28

    Dietary supplement Arize recalled for undeclared pharmaceutical ingredient

    Arize Herbal Dietary Supplement contains an undeclared ingredient (nortadalafil), a pharmaceutical used in FDA-approved male sexual enhancement medications, making it an unapproved drug.

    Product
    Arize Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Natural Herbal Remedies, LLC, Cheyenne, WY 82001, www.getarize.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1082-2024·2024-02-28

    Medical Closure Kit Recall: Sterility of Saline Cannot Be Guaranteed

    Windstone Medical Packaging is recalling Aligned Medical Solutions Closure Kits due to inability to guarantee sterility of included saline. This FDA Class I recall affects 475 units distributed in Florida, Illinois, and California.

    Product
    Aligned Medical Solutions, Closure Kit, AMS13043, STERILEEO
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1049-2024·2024-02-28

    Dover Irrigation Convenience Kits Recalled for Component Defects

    Cardinal Health is recalling Dover Irrigation convenience kits that contained components which were separately recalled. The recall affects over 63,000 units distributed across the US, EMEA, Japan, and Latin America.

    Product
    Dover" IRRIGATION 1200 CC TRAY, 60 CC PISTON SYRINGE, STERILE SALINE, TIP PROTECTOR, ALCOHOL, LIDDED
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1051-2024·2024-02-28

    Cardinal Health Foley Catheter Kits Recalled Over Supplier Component Defect

    Cardinal Health is recalling 36,300 Foley urinary drainage convenience kits due to components that were subsequently recalled by supplier Nurse Assist.

    Product
    Dover" 100% SILICONE 400ML U/M TEMP SENSE FOLEY TRAY, LL, 18 FR (6.0 MM), 5CC, 2000ML DRAIN BAG, CSD
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·24V158000·2024-02-28

    Jayco Recalls 2024 Motorhomes Due to Rear Axle Lubricant Defect

    Jayco is recalling 2024 Entegra and Jayco motorhomes because inadequate rear axle lubricant may cause bearing damage, leading to wheel lock-up or driveshaft separation.

    Product
    ENTEGRA — ENTEGRA, JAYCO CONDOR, SOLSTICE, EXPANSE LI, EXPANSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1079-2024·2024-02-28

    Surgical Kit with Saline Recalled Over Sterility Assurance Issue

    Windstone Medical Packaging is recalling a surgical kit due to inability to guarantee sterility of the included saline. The recall affects 1,528 units distributed in Florida, Illinois, and California.

    Product
    Aligned Medical Solutions, Local Lower Extremity Pack I, AMS10833, STERILEEO
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1001-2024·2024-02-28

    Baxter Exactamix Pro 1200 Software Error Causes Medication Over-delivery

    Baxter Healthcare is recalling the Baxter Exactamix Pro 1200 medication compounding device due to a software error that may cause ingredient over-delivery when using the 'Use Some Overfill' feature.

    Product
    Baxter Exactamix Pro 1200, REF EXM12DY
    Category
    Medical Device
    Distribution
    22 states
  • SevereFDA (Food)·F-0910-2024·2024-02-28

    Ham and Cotija Torta Sandwiches Recalled for Listeria Contamination

    Compass Group USA, Inc. is recalling 206 Ham & Cotija Torta Sandwiches due to Listeria monocytogenes contamination in Cotija cheese. Products were distributed in Florida with use-by dates of February 9-16, 2024.

    Product
    Ham & Cotija Torta Sandwich on Telera Roll, 8.3 oz, plastic container, UPC 100001002017
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·24V156000·2024-02-28

    Nissan Rogue seat belt pretensioners may not restrain occupants properly

    Nissan is recalling certain 2023 Rogue vehicles because incorrectly manufactured driver and front passenger seat belt pretensioners may fail to restrain occupants, breaching FMVSS 208, 209 and 210.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1047-2024·2024-02-28

    Dover Foley catheters recalled due to defective supplied components

    Cardinal Health Dover Foley catheters (7,800 units distributed in the US, EMEA, Japan, and Latin America) are being recalled because convenience kits were manufactured with components previously recalled by Nurse Assist.

    Product
    Dover" HYDROGEL COATED LATEX 400 ML U/M FOLEY TRAY, LL, 14 FR (4.7 MM), 5 CC, 2000 ML DRAIN BAG, CSD; Dover" 100% SILICONE SILVER-HYDROGEL COATED 400ML U/M TEMP SENSE FOLEY TRAY, 16FR (5.3 MM), 5CC, CSD; Dover" 100% SILICONE SILVER-HYDROGEL COATED 400ML U/M TEMP SENSE FOLEY TRAY
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1048-2024·2024-02-28

    Dover Foley catheter convenience kits recalled due to component defects

    Cardinal Health is recalling Dover-branded Foley catheter convenience kits with components that were subsequently recalled by Nurse Assist. The recall affects 195,600 units distributed in the US, EMEA region, Japan, and Latin America.

    Product
    Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, COUD¿ TIP, 16 FR (5.3 MM), 5 CC, 2000 ML DRAIN BAG; Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, COUD¿ TIP, 18 FR (6.0 MM), 5 CC, 2000 ML DRAIN BAG; Dover" HYDROGEL COATED LATEX FOLEY TRAY, LUER LOCK, 16 FR (5.3 MM), 5 CC, 2000 ML BAG, D
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1043-2024·2024-02-28

    Argyle Suction Catheter Trays with Chimney Valve recalled for defective components

    Cardinal Health is recalling multiple Argyle Suction Catheter Tray models due to defective components. The kits containing these recalled components were distributed in the US, Europe, Japan, and Latin America.

    Product
    Argyle" Suction Catheter Tray with Chimney Valve Sterile Saline 18 Fr/Ch (6.0mm); Argyle" Suction Catheter Tray with Chimney Valve Sterile Saline, 6 Fr/Ch (2.0 mm); Argyle" Graduated Suction Catheter Tray with Chimney Valve Sterile Saline 8 Fr/Ch (2.67 mm); Argyle" Suction Cathet
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1045-2024·2024-02-28

    Dover Foley Catheter and Urinary Drainage Kits Recalled for Defective Components

    Cardinal Health is recalling Dover foley catheter and urinary drainage kits containing components previously recalled by supplier Nurse Assist. The FDA Class I recall affects 17,640 units distributed to the US, EMEA, Japan, and Latin America.

    Product
    Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, NEEDLE PORT, 16 FR (5.3 MM), 5 CC, 2000 ML DRAIN BAG; Dover" HYDROGEL COATED LATEX 400 ML U/M FOLEY TRAY, NEEDLE, 16 FR (5.3 MM), 5 CC, 2000 ML BAG; Dover" UNIVERSAL TRAY, 1000 ML BASIN, PVP SOLUTION, PREPPING COMPONENTS, 10 ML PRE-FILL
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0346-2024·2024-02-28

    TING Athlete's Foot Spray Recalled Due to Benzene Contamination

    Insight Pharmaceuticals is recalling TING 1% Tolnaftate Athlete's Foot Spray due to benzene contamination. The recall affects approximately 59,644 cans distributed nationwide.

    Product
    TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid, NET WT 4.5 oz. (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591 UPC 3 63736 81961 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0335-2024·2024-02-28

    Neptune's Fix Tianeptine Tablets Recalled for FDA Unapproved Marketing

    Neptune's Fix Tianeptine Tablets are being recalled because the product contains tianeptine, a substance not approved by the FDA for any medical use. The recall affects 4,932 boxes distributed nationwide.

    Product
    Neptune's Fix, Tianeptine Tablets Extended Relief, Twenty Tablets per Box, Wide Awake, 3000 mg (150 mg Per Tablet), Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0333-2024·2024-02-28

    FDA Recalls Neptune's Fix Tianeptine Elixir for Containing Unapproved Drug

    Neptune's Fix Tianeptine Elixir has been recalled because it contains tianeptine, an unapproved drug substance in the United States. Approximately 1 million bottles distributed nationwide are affected.

    Product
    Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl oz (10 mL) bottle, Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1044-2024·2024-02-28

    Tracheostomy Supply Kits Recalled for Defective Components

    Cardinal Health is recalling 661,560 tracheostomy kits because they were manufactured with components that were subsequently recalled by another manufacturer.

    Product
    TRACH KIT W/HYDROGEN & SALI
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1143-2024·2024-02-28

    Ionolux dental cement recalled for manufacturing defect affecting curing

    Ionolux dental cement capsules may contain incorrect plungers that prevent proper curing. Affected batches distributed in the US and internationally should not be used.

    Product
    Ionolux, Catalog (REF) Numbers: a) 2115, b)2117, c) 2118, d) 2119, e) 2120, f) 2122; dental cement
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1177-2024·2024-02-28

    Azurion 5 X-Ray System Generator May Fail Due to Circuit Short

    Philips Azurion 5 X-ray systems with Certeray generators may experience power loss due to a potential short circuit in the power inverter board, potentially delaying or interrupting medical procedures.

    Product
    Azurion 5 with a Certeray generator-To perform image guidance in diagnostic, interventional, and minimally invasive surgery procedures Models: (1) 722227 (2) 722228
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0340-2024·2024-02-28

    Prescription injection drug recalled due to temperature excursion during shipment

    Acthar Gel (repository corticotropin injection) is being recalled due to a temperature excursion during shipping from the manufacturer to distributor. Lot #1564-103 should not be dispensed to patients.

    Product
    ACTHAR — ACTHAR (REPOSITORY CORTICOTROPIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1179-2024·2024-02-28

    Biliary Endoprosthesis Labeling Mismatch Risks Incorrect Device Placement

    W.L. Gore's GORE VIABIL Short Wire Biliary Endoprosthesis may be mislabeled regarding drainage holes, risking extended procedures, infections, and unplanned device removal in 24 units distributed in Georgia.

    Product
    GORE VIABIL Short Wire Biliary Endoprosthesis, Product labeled as (1) Catalog Number VSWVH1008, 10 mm x 8 cm; with holes; and (2) Catalog Number VSWVN1008, 10 mm x 8 cm; no holes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1146-2024·2024-02-28

    Henry Schein Criterion Level 3 Earloop Masks Recalled for Non-Validated Equipment

    AMD Medicom Inc. is recalling Henry Schein Criterion Level 3 Earloop Masks because they were produced on non-validated equipment not included in the initial product qualification.

    Product
    HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0889-2024·2024-02-28

    Bulk Baking Ingredient Recalled for Potential Foreign Material Contamination

    Mennel Milling Company is recalling SPECIAL CAKE 53869 bulk ingredient due to potential contamination with metal, wood, and other foreign material. Affected product was distributed in six states.

    Product
    SPECIAL CAKE 53869 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Drugs)·D-0332-2024·2024-02-28

    Equate Cherry Cough Drops recalled for potential glass and silicone contamination

    Bestco LLC is recalling Equate Cherry Cough Drops nationwide due to potential glass and silicone particulates from manufacturing deviations. Affected products are 30-drop and 160-drop bags expiring December 31, 2026.

    Product
    Equate Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, a) 30 drops per bag, item number 20000462, b) 160 drops per bag, item number 20000463, Bestco, 288 Mazeppa Road, Mooresville, NC 28115
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1150-2024·2024-02-28

    Epidural Tray Kits Recalled for Wrong Connector Type

    B. Braun Medical recalls 3,890 PERIFIX epidural trays nationwide due to filter straws with incompatible neuraxial connectors instead of standard Luer connectors.

    Product
    Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy, 5 mL Glass Luer Lock LOR Tray (Kit) A collection of devices intended for the administration of an analgesic or anesthetic agent to the epidural space for the management of pain. It includes the pharmaceutical anestheti
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0912-2024·2024-02-28

    Country Corner Dairy White Colby Cheese Recalled for Improper Pasteurization

    Country Corner Dairy is recalling WHITE COLBY CHEESE products due to improper pasteurization. The recalled products were distributed to Maryland and Virginia.

    Product
    Fresh Local , Country Corner Dairy, WHITE COLBY CHEESE, INGREDIENTS: Pasteurized Milk, Salt , Rennet, Calcium Chloride, Cheese Culture, Contains Milk. Product comes in various sizes, 6 oz. up to 42 lbs. and is in vacuum sealed plastic packaging.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0326-2024·2024-02-28

    Fluticasone Propionate Nasal Spray Recalled for Potential Bacterial Contamination

    Apotex Corp. is recalling Fluticasone Propionate Nasal Spray (292,752 bottles nationwide) due to potential Burkholderia cepacia contamination from manufacturing deviations. No illnesses reported.

    Product
    FLUTICASONE PROPIONATE — FLUTICASONE PROPIONATE (FLUTICASONE PROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1174-2024·2024-02-28

    Aquabiliti saline flush syringes recalled for potential sodium chloride content deficiency

    MRP, LLC is recalling AQUABILITI AQUASTAT saline flush syringes because they may fail to meet USP standards for sodium chloride content after 12 months.

    Product
    AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe, USP, 5mL in 12mL, REF 2T0805; and 3mL in 12mL, REF 2T0807, intermediate cartons containing 100 syringes, shipping cases containing 400 syringes, Rx, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0330-2024·2024-02-28

    Kroger Cherry Cough Drops recalled for potential glass and silicone contamination

    Bestco LLC is recalling Kroger Cherry Cough Drops due to potential glass and silicone particulates in the product. The recall affects product distributed nationwide.

    Product
    Kroger Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per bag, item number 20000064, Bestco, 288 Mazeppa Road, Mooresville, NC 28115
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0900-2024·2024-02-28

    Bulk Animal Feed Recalled for Potential Foreign Material Contamination

    Mennel Milling Company is recalling non-human consumption feed products due to potential contamination with metal, wood, and gasket material. Approximately 2.6 million pounds were distributed across six states.

    Product
    NON-HUMAN CONSUMPTION delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1154-2024·2024-02-28

    X-Ray C-Arm System Internal Board Defect Causes Abnormal Images

    Canon Medical System X-ray C-arm systems may display abnormal images due to an internal board manufacturing defect, potentially preventing exam completion and requiring patients to be re-examined with alternative equipment.

    Product
    The device is an X-ray system that is capable of radiographic and fluoroscopic studies and is used in an interventional setting. The system consists of a C-arm which is equipped with an X-ray tube, beam limiter and X-ray receptor, X-ray controller, computers with system and proce
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0880-2024·2024-02-28

    Flour recalled for potential metal and foreign material contamination

    Mennel Milling Company is recalling flour products due to potential contamination with metal, wood, gasket material, and sifter balls. Affected product was distributed in Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.

    Product
    160919 FLR BLE WINTER delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0892-2024·2024-02-28

    Flour Product Recall Due to Foreign Material Contamination

    Mennel Milling Company is recalling 2.6 million pounds of bulk AP flour that may contain metal, wood, gasket material, and sifter balls. The flour was distributed in six states and should not be used.

    Product
    01050 KA AP FLOUR delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0891-2024·2024-02-28

    Bulk Milling Product Recalled for Metal and Foreign Material Contamination

    Mennel Milling Company is recalling 2.6 million pounds of bulk milling product due to potential contamination with metal, wood, gasket material, and sifter balls. The product was distributed in six states; no illnesses or injuries have been reported.

    Product
    9200458510 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Drugs)·D-0329-2024·2024-02-28

    Meijer Cherry Cough Drops recalled for potential glass and silicone contamination

    Bestco LLC is recalling Meijer Cherry Cough Drops due to potential glass and silicone particulates found during manufacturing quality control inspections. Consumers should stop using the product immediately.

    Product
    Meijer Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per bag, item number 20000345, Bestco, 288 Mazeppa Road, Mooresville, NC 28115
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0897-2024·2024-02-28

    Pizza Flour Recalled for Potential Foreign Material Contamination

    Mennel Milling Company is recalling pizza flour due to potential contamination with metal, wood, gasket material, and sifter balls. Approximately 2.6 million pounds were distributed across Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.

    Product
    PIZZA FLOUR EN MA BL delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0881-2024·2024-02-28

    Bulk animal feed product recalled for potential foreign material contamination

    Mennel Milling Company is recalling 2ND CLEAR 1051664, a bulk animal feed product, due to potential contamination with metal, wood, gasket material, and sifter balls. Affected products were distributed in Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.

    Product
    2ND CLEAR 1051664 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1169-2024·2024-02-28

    3M Surgical Blade Assembly Recalled for Burn Injury Risk During Use

    3M is recalling the Specialty Blade Assembly (REF 9660) used with 3M Surgical Clippers worldwide due to burn risk if the blade overheats during operation. Approximately 52.8 million units affected across all lot codes.

    Product
    3M Specialty Blade Assembly, REF 9660,70-2011-8462-2, 7100213114, used with used with 3M Surgical Clipper Catalog Number 9661L
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0893-2024·2024-02-28

    Bulk Product Recalled for Potential Metal, Wood, and Foreign Material Contamination

    Mennel Milling Company is recalling bulk product 2-00007-0000 due to potential contamination with metal, wood, gasket material, and sifter balls. The product was distributed in Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.

    Product
    2-00007-0000 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0908-2024·2024-02-28

    Spice product recalled for undeclared wheat allergen

    Vandevi Compounded Asafoetida spice is recalled due to undeclared wheat. Consumers with wheat allergies should not use this product.

    Product
    Vandevi Compounded Asafoetida 50 gm, 100 gms 200 gm, 500 gm, 1 kg. Packaged in yellow plastic bottles with plastic shrink wrap blue/yellow labels.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1170-2024·2024-02-28

    3M Surgical Clipper Blade Assembly Recalled Due to Burn Risk

    3M recalled 764,580 Specialty Blade Assemblies for surgical clippers due to risk of burns from overheating. The blade can reach temperatures exceeding 77°C if left running improperly.

    Product
    3M Specialty Blade Assembly, REF 9660,70-2011-8491-1, 7100213026, used with used with 3M Surgical Clipper Catalog Number 9661L
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0339-2024·2024-02-28

    Fosfomycin Tromethamine Granules Recalled for Out-of-Specification Organic Impurities

    Ascend Laboratories recalls 71,244 sachets of Fosfomycin Tromethamine for failing quality specifications due to organic impurities. Patients with affected lots should consult their healthcare provider.

    Product
    FOSFOMYCIN TROMETHAMINE — FOSFOMYCIN TROMETHAMINE (FOSFOMYCIN TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0887-2024·2024-02-28

    Pizza 50/50 Unmalted Flour Recalled for Potential Foreign Material

    Mennel Milling Company is recalling approximately 2.6 million pounds of PIZZA 50/50 UNMALTED flour due to potential contamination with metal, wood, gasket material, and sifter balls.

    Product
    PIZZA 50/50 UNMALTED delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0883-2024·2024-02-28

    Bagel Flour Recalled Due to Potential Foreign Material Contamination

    Mennel Milling Company is recalling approximately 2.6 million pounds of bagel flour distributed in six states due to potential contamination with metal, wood, gasket material, and sifter balls.

    Product
    BAGEL FLOUR delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0888-2024·2024-02-28

    Spring Flour Recalled for Potential Metal and Wood Contamination

    Mennel Milling Company is recalling R01001 ENR SPRING FLR flour due to potential contamination with metal, wood, gasket material, and sifter balls. Consumers should not use affected product.

    Product
    R01001 ENR SPRING FLR delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0886-2024·2024-02-28

    HARD E6 1036 bulk product recalled for foreign material contamination

    Mennel Milling Company is recalling HARD E6 1036 bulk product distributed across six states due to potential contamination with metal, wood, gasket material, and sifter balls. No illnesses have been reported.

    Product
    HARD E6 1036 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0890-2024·2024-02-28

    Malted Flour Recalled for Potential Foreign Material Contamination

    Mennel Milling Company recalls UNBLE ENR MALTED RM6144 FLOUR for potential foreign material contamination including metal, wood, gasket material, and sifter balls. The recall affects approximately 2.6 million pounds distributed in six states.

    Product
    UNBLE ENR MALTED RM6144 FLOUR delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0895-2024·2024-02-28

    FDA Recalls Bulk Milling Product for Potential Foreign Material

    Mennel Milling Company is recalling its milling product (2-15969-0000) due to potential contamination with metal, wood, gasket material, and sifter balls. The product was distributed across Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.

    Product
    2-15969-0000 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0915-2024·2024-02-28

    Country Corner Dairy Sizzling Colby Cheese Recalled Due to Improper Pasteurization

    Country Corner Dairy is recalling Sizzling Colby Cheese due to lack of proper pasteurization. The recalled product was distributed in Maryland and Virginia.

    Product
    Fresh Local , Country Corner Dairy, SIZZLING COLBY CHEESE, INGREDIENTS: Pasteurized Milk, Salt , Rennet, Calcium Chloride, Cheese Culture, Peppers, Contains Milk. Product comes in various sizes, 6 oz. up to 42 lbs. and is in vacuum sealed plastic packaging.
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·24V157000·2024-02-28

    Commercial truck camera cable routing can damage wiring and cause fire

    Isuzu is recalling certain FTR, FVR and Chevrolet LCF trucks with Mobileye Collision Warning Systems because a misrouted camera cable can damage wiring and overload the electrical circuit.

    Product
    CHEVROLET — CHEVROLET, ISUZU 7500XD, 6500XD, FTR, FVR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0878-2024·2024-02-28

    Donut Cake Flour Recalled for Potential Metal and Foreign Material Contamination

    Mennel Milling Company is recalling donut cake flour products due to potential contamination with metal, wood, gasket material, and sifter balls. The affected product was distributed across six states; no illnesses have been reported.

    Product
    1002560 DONUT CAKE FLR delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0879-2024·2024-02-28

    Flour Recalled for Potential Foreign Material Contamination

    Mennel Milling Company is recalling approximately 2.6 million pounds of ALL PURPOSE EN EZ BL flour due to potential contamination with metal, wood, gasket material, and sifter balls.

    Product
    15953 ALL PURPOSE EN EZ BL delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0877-2024·2024-02-28

    Mennel Milling White Flour Recalled for Potential Foreign Material

    Mennel Milling Company is recalling white flour delivered as bulk product due to potential contamination with metal, wood, gasket material, and sifter balls. The recall affects approximately 2.6 million pounds distributed across six states.

    Product
    1000000 White Flour UNBL EN MT delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1178-2024·2024-02-28

    Azurion 7 Medical Imaging System May Lose Power During Procedures

    Philips Azurion 7 imaging systems may experience power loss due to a potential short circuit in the power inverter, risking delays or termination of diagnostic and surgical procedures.

    Product
    Azurion 7 with a Certeray generator-To perform image guidance in diagnostic, interventional, and minimally invasive surgery procedures Models: (1) 722223, (2) 722224, (3) 722225, (4) 722226
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0914-2024·2024-02-28

    Country Corner Dairy Yellow Cheddar Cheese Recall Due to Improper Pasteurization

    Country Corner Dairy is recalling Yellow Cheddar Cheese due to lack of proper pasteurization. The product was distributed in Maryland and Virginia and may pose a food safety risk.

    Product
    Fresh Local , Country Corner Dairy, YELLOW CHEDDAR CHEESE, INGREDIENTS: Pasteurized Milk, Salt , Rennet, Calcium Chloride, Cheese Culture, Color, Contains Milk. Product comes in various sizes, 6 oz. up to 42 lbs. and is in vacuum sealed plastic packaging.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0911-2024·2024-02-28

    Country Corner Dairy White Cheddar Cheese Recalled for Improper Pasteurization

    Country Corner Dairy white cheddar cheese from Maryland and Virginia is being recalled due to inadequate pasteurization during manufacturing. The product was distributed in various sizes in vacuum-sealed packaging.

    Product
    Fresh Local , Country Corner Dairy, WHITE CHEDDAR CHEESE, INGREDIENTS: Pasteurized Milk, Salt , Rennet, Calcium Chloride, Cheese Culture, Contains Milk. Product comes in various sizes, 6 oz. up to 42 lbs. and is in vacuum sealed plastic packaging.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0901-2024·2024-02-28

    Animal feed recalled for potential foreign material contamination

    Mennel Milling Company recalled PB AP bulk animal feed due to potential contamination with metal, wood, gasket material, and sifter balls. Approximately 2.6 million pounds of affected product was distributed across six states.

    Product
    PB AP delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0884-2024·2024-02-28

    Bread Flour Recalled for Potential Foreign Material Contamination

    Mennel Milling Company is recalling bulk bread flour due to potential contamination with metal, wood, gasket material, and sifter balls. The flour was distributed to bakeries and food manufacturers in six states.

    Product
    BREAD FLOUR UNBL ENR delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0885-2024·2024-02-28

    Mennel Milling Company Recalls Dried Grain Product for Foreign Material Contamination

    Mennel Milling Company is recalling approximately 2.6 million pounds of DRIED SOFT 75 ENR 134348 due to potential contamination with metal, wood, gasket material, and sifter balls.

    Product
    DRIED SOFT 75 ENR 134348 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0902-2024·2024-02-28

    Pizza 50/50 Flour Recalled for Potential Metal, Wood, and Foreign Material

    Mennel Milling Company recalls Pizza 50/50 Unmalted flour due to potential metal, wood, gasket material, and sifter ball contamination. The affected product was distributed across KY, MI, NJ, NY, and PA.

    Product
    PIZZA 50/50 UNMALTED 904181 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0896-2024·2024-02-28

    Wheat Flour Recalled for Potential Foreign Material Contamination

    Mennel Milling Company is recalling bleached wheat flour due to potential contamination with metal, wood, gasket material, and sifter balls. The product was distributed across six states.

    Product
    BLEACHED WHEAT FLOUR 5600352 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0882-2024·2024-02-28

    Bread Flour Recalled for Potential Metal and Foreign Material Contamination

    Mennel Milling Company is recalling approximately 2.6 million pounds of bread flour due to potential contamination with metal, wood, gasket material, and sifter balls. Affected flour was distributed in six states.

    Product
    43058751 BREAD FLR delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0904-2024·2024-02-28

    Bulk Fortune Cookies Recalled for Undeclared Wheat and Soy

    New World Company is recalling bulk cases of Fortune cookies distributed in California due to undeclared wheat and soy allergens that pose a risk to consumers with these allergies.

    Product
    Bulk case of Fortune cookies, labeled as 6 lb (1.3 lb per bag/ 4 bags per case)
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0913-2024·2024-02-28

    Country Corner Dairy Yellow Colby Cheese Recalled for Improper Pasteurization

    Country Corner Dairy is recalling Yellow Colby Cheese distributed in Maryland and Virginia due to insufficient pasteurization during manufacturing.

    Product
    Fresh Local , Country Corner Dairy, YELLOW COLBY CHEESE, INGREDIENTS: Pasteurized Milk, Salt , Rennet, Calcium Chloride, Cheese Culture, Contains Milk. Product comes in various sizes, 6 oz. up to 42 lbs. and is in vacuum sealed plastic packaging.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0898-2024·2024-02-28

    Hard Wheat Flour Recalled for Potential Metal and Wood Contamination

    Mennel Milling Company is recalling hard wheat flour distributed in six states due to potential contamination with metal, wood, gasket material, and sifter balls. Approximately 2.6 million pounds of product may be affected.

    Product
    HARD WHEAT 2ND CLEAR delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0905-2024·2024-02-28

    Fortune Cookies Recalled Due to Undeclared Soy Allergen

    Fortune cookies from New World Company are recalled for containing undeclared soy allergen. The 1 lb retail bags were distributed in California to consumers.

    Product
    Fortune cookies, 1 lb plastic retail bags
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0906-2024·2024-02-28

    Fortune cookies recalled for undeclared soy allergen

    Fortune cookies manufactured by New World Company are being recalled due to undeclared soy allergen. Consumers with soy allergies should not consume the product.

    Product
    Fortune cookies, individually wrapped in a 6lb case, 190 pcs / case
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1145-2024·2024-02-28

    Philips Azurion Interventional X-ray Systems framegrabber card may fail to display images

    The framegrabber card in Philips Azurion interventional X-ray systems may fail to display diagnostic images properly, potentially delaying procedures.

    Product
    Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of the affected system. Affected PCs: FlexViewing PC Azurion Model Name - Model Number: Azurion 7 B12 722067; Azurion 7 B20 722068; Azurion 7 M12 722078 722223;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0899-2024·2024-02-28

    Mennel Milling I-52 Patent Flour Recalled for Foreign Material Contamination

    Mennel Milling Company recalled I-52 Patent Flour containing potential foreign material including metal, wood, gasket material, and sifter balls. The flour was distributed in bulk trailers across six states.

    Product
    I-52 PATENT FLOUR delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighUSDA FSIS·008-2024·2024-02-28

    M&P Production Recalls Raw Lamb and Beef Samsa for Undeclared Sesame

    M&P Production LTD is recalling raw lamb and beef samsa products because they contain sesame seeds, a known allergen, that are not declared on the label.

    Product
    M&P Production LTD — M&P Production LTD Recalls Raw Lamb and Beef Samsa Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    4 states

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