The Recall Desk

Archive

July 2023 recalls

787 recalls were announced in July 2023.

What the numbers show

Critical
65
Severe
365
High
307
Moderate
50

Of the 787 recalls this month scored against our rubric, 8% are Critical, 46% are Severe.

Which agencies issued them

201–300 of 787

  • SevereFDA (Food)·F-1243-2023·2023-07-19

    Multiple Brands of Dill Pickle Pretzels Recalled for Undeclared Milk

    Dakota Style, Inc. is recalling multiple brands of dill pickle pretzels nationwide because they may contain undeclared milk, a major allergen. Consumers with milk allergies should not consume these products.

    Product
    1. Hy-Vee Dill Pickle Braided Pretzels, 10oz poly bags, UPC: UPC: 75450-24308, 12 pack; 2. Schnucks Dill Pickle Pretzel Schticks, 10oz poly bags, UPC: 41318-25268, 12 pack; 3. Best Choice Dill Pickle Pretzel Twists, 10oz poly bags, UPC: 700038-66480, 12 pack; 4. Gelson's Dill P
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V497000·2023-07-19

    Vanguard Recalls 2023-2024 Trailers with Tire Inflation System Defect

    Vanguard is recalling 2023-2024 trailers equipped with a specific tire inflation system that may cause tires to deflate, increasing crash risk.

    Product
    VANGUARD — VANGUARD VTD TRAILER, MAXCUBE, VSD TRAILER, VIP 4000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1244-2023·2023-07-19

    Gelson's Sea Salt Pretzels Recalled for Undeclared Milk Allergen

    Gelson's Sea Salt Pretzels are being recalled nationally because they may contain undeclared milk. This poses a hazard to consumers with milk allergies.

    Product
    Gelson's Sea Salt Pretzels, 4.5oz poly bags, UPC: 23631-11185, 12 pack
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1238-2023·2023-07-19

    Mini Deviled Crabs recalled for undeclared milk and sesame allergens

    SANTOS FROZEN FOODS is recalling Mini Deviled Crabs, 1oz, due to undeclared milk and sesame seeds. Consumers with allergies to these allergens should not consume the product.

    Product
    Mini Deviled Crabs, 1oz
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1231-2023·2023-07-19

    Frozen strawberries recalled for potential Hepatitis A contamination

    Wawona Frozen Foods recalls Organic Daybreak Blend frozen strawberries sold at Costco due to potential Hepatitis A. Approximately 9,878 cases were distributed to Costco locations in five western states with lot codes dated through October 2023.

    Product
    Organic Daybreak Blend Brand Name: Wawona Frozen Foods 4 lb. plastic bags - 10 bags per case Keep Frozen Item# 684779 UPC: 0 34742 07244 5 Sold by Costco
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-1239-2023·2023-07-19

    Frozen Deviled Crabs Recalled for Undeclared Milk and Sesame Seeds

    SANTOS FROZEN FOODS is recalling Regular Deviled Crabs (4oz) for undeclared milk and sesame allergens. Approximately 520 cases were distributed domestically in affected lots beginning with 23 and ending in 03, 04, or 05.

    Product
    Regular Deviled Crabs, 4oz
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1232-2023·2023-07-19

    Great Value Sliced Strawberries recalled for potential Hepatitis A contamination

    Walmart's Great Value Sliced Strawberries are being recalled due to potential Hepatitis A contamination. Approximately 28,650 bags distributed across 32 states are affected.

    Product
    Great Value Sliced Strawberries. Item # 107356. Frozen, packaged flexible plastic bags. Net wt. 4 lbs (64oz). UPC on retail bag: 0 78742 25387 9. A total of 6 sellable units (4lbs. each) are placed into a case for distribution to retailer. DISTRIBUTED BY: Walmart Inc. Bentonvi
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1241-2023·2023-07-19

    Pretzel products recalled for undeclared milk allergen nationwide

    Dakota Style, Inc. is recalling salt and vinegar pretzel products nationwide because they may contain undeclared milk. Consumers with milk allergies should not consume these products.

    Product
    1. Hy-Vee Salt & Vinegar Braided Pretzels, 10 oz poly bags, UPC: UPC: 75450-27706, 12 pack; 2. Dakota Style Salt & Vinegar Pretzel Kravings, 4.5 oz poly bags, UPC: 84872-60030, 6 pack; 3. Dakota Style Salt & Vinegar Pretzel Kravings, 10 oz poly bags, UPC 84872-60018, 12 pack, 4
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1245-2023·2023-07-19

    Tampico Brand Mango Punch Recalled for Undeclared Yellow 5 Dye

    Tampico brand Mango Punch (1 gallon) is recalled because it contains undeclared Yellow 5, a food dye that can cause reactions in people with tartrazine sensitivity.

    Product
    Tampico brand Mango Punch; LESS THAN 1% JUICE; 1 GAL (3.78 L); INGREDIENTS: WATER, HIGH FRUCTOSE CORN SYRUP, LESS THAN 2% OF MANGO JUICE FROM CONCENTRATE, ORANGE JUICE FROM CONCENTRATE, TANGERINE JUICE FROM CONCENTRATE, ASCORBIC ACID (VITAMIN C), NATURAL AND ARTIFICIAL FLAVORS, P
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1247-2023·2023-07-19

    1st Phorm Level-1 Protein Supplement Recalled for Potential Staphylococcus aureus

    International Food Companies is recalling 1st Phorm Level-1 Sustained Assimilation Protein (Milk Chocolate) due to potential Staphylococcus aureus contamination. Consumers should not consume the product.

    Product
    1st phorm Level-1 Sustained Assimilation Protein. Milk Chocolate. Protein Supplement. Item number 502066. Net Wt. 2.45 lbs (1.11kg) UPC 8 50026-19672 6. Manufactured & Designed Exclusively for 1st Phorm, 2091 Fenton Logistics Pk Blvd, Fenton, MO 63026
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2133-2023·2023-07-19

    Medline Non-Sterile PVP Solution Kits Mislabeled as Sterile

    Medline is recalling Total Knee Theda surgical kits where the non-sterile PVP solution was mislabeled as sterile. Healthcare providers should immediately stop using the recalled kits and contact Medline.

    Product
    MEDLINE NON-STERILE PVP SOLUTION, packaged in kits as follows: TOTAL KNEE THEDA, Model Number DYNJ908683A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0911-2023·2023-07-19

    Fexofenadine Tablets Recalled for Failed Impurity and Degradation Specifications

    L. Perrigo Company is recalling Picnic Fexofenadine Hydrochloride Tablets (180 mg) nationwide because the product failed impurity and degradation specifications. The affected lot is 2DR0471 with expiration date 12/23.

    Product
    Picnic, Fexofenadine Hydrochloride Tablets, 180 mg, Antihistamine, 90-count cartons, Distributed by: Thirty Madison, Inc., New York, NY 10001. NDC 45 tablets: 80159-112-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2134-2023·2023-07-19

    Medline Non-Sterile PVP Solution Mislabeled as Sterile

    Medline Industries is recalling 128 units of non-sterile PVP solution incorrectly labeled as sterile. Using a non-sterile product in sterile contexts could create infection risk.

    Product
    MEDLINE NON-STERILE PVP SOLUTION, packaged in kits as follows: OISC HAND BEAR, Model Number DYNJ902348L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2131-2023·2023-07-19

    Medline PVP solution mislabeled as sterile when non-sterile

    Medline Industries is recalling batches of non-sterile PVP solution that were incorrectly labeled as sterile, creating risk of inadvertent use in sterile medical settings.

    Product
    MEDLINE NON-STERILE PVP SOLUTION, STERILE PACKAGING REF DYNDA2232A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2124-2023·2023-07-19

    Ultrasound Device Boot Failure May Delay Emergency Availability

    Certain GE HealthCare Vivid S60 ultrasound systems may not boot up in a timely fashion, potentially delaying device availability in time-critical emergency situations.

    Product
    GE Healthcare Vivid S60, ultrasound device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0907-2023·2023-07-19

    Fexofenadine Hydrochloride Tablets Recalled for Failed Purity Specifications

    L. Perrigo Company is recalling 15,504 cartons of Fexofenadine Hydrochloride 180 mg tablets nationwide due to failed impurity and degradation specifications.

    Product
    FEXOFENADINE HYDROCHLORIDE — FEXOFENADINE HYDROCHLORIDE (FEXOFENADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0909-2023·2023-07-19

    Allergy Relief Fexofenadine Tablets Recalled for Failed Impurity Specifications

    L. Perrigo's Allergy Relief 180 mg tablets are being recalled due to failed impurity and degradation specifications. The recall affects 32,904 cartons distributed nationwide.

    Product
    ALLERGY RELIEF — ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2121-2023·2023-07-19

    Medtronic Catalyft LS Spinal Implant Recall Due to Out-of-Specification Geometry

    Medtronic recalls 10 units of Catalyft LS spinal implants due to potential out-of-specification device geometries. The affected implants may not properly support or accommodate patient anatomy during lumbar fusion surgery.

    Product
    Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981027722, spinal implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2108-2023·2023-07-19

    Osteomed AutoDrive Screws Recalled for Undersized Screw Head

    Osteomed recalls orthopedic AutoDrive screws used in osteotomy procedures due to undersized screw heads that could pass through the mounting plate hole, potentially affecting surgical fixation.

    Product
    REF 218-1604-SP-10, Profile 0 4mm AutoDrive Screw Sterile Qty 10, Rx Only, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2135-2023·2023-07-19

    Medline Non-Sterile PVP Solution Incorrectly Labeled as Sterile

    Medline is recalling Non-Sterile PVP Solution Hystero Pack kits due to mislabeling: affected lots labeled as 'Sterile' when actually 'Non-Sterile'. Using non-sterile solution in sterile gynecological procedures creates infection risk.

    Product
    MEDLINE NON-STERILE PVP SOLUTION, packaged in kits as follows: HYSTERO PACK, Model Number DYNJ61448A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0897-2023·2023-07-19

    Sunmark and Generic Eye Drops Recalled for Manufacturing Deficiency

    K.C. Pharmaceuticals is recalling 341,568 bottles of Sunmark and generic tetrahydrozoline eye drops due to manufacturing practice deficiencies. The recall affects multiple brands distributed nationwide.

    Product
    SUNMARK EYE DROPS ORIGINAL FORMULA — SUNMARK EYE DROPS ORIGINAL FORMULA (TETRAHYDROZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0916-2023·2023-07-19

    Sodium Chloride Injection Bags Recalled for Potential Leakage and Sterility Risk

    B. Braun Medical Inc. is recalling 79,880 bags of Sodium Chloride Injection due to potential leakage that could compromise sterility. No illnesses or injuries have been reported.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0915-2023·2023-07-19

    Hand Sanitizer Recalled for Impurities Exceeding Allowable Limits

    Big Machine Distillery Hand Sanitizer is being recalled due to manufacturing impurities exceeding allowable limits. No illnesses or injuries have been reported.

    Product
    Big Machine Distillery Hand Sanitizer Non-Sterile Solution Alcohol Antiseptic 80% Topical Solution, Produced and Distributed by Big Machine Distillery 1800 Abernathy Road Lynnville, TN 38472 a) 50 mL UPC 8 59105 00452 5; b) 100 mL UPC 8 59105 00453 2; c) 375 mL; d) 1/2 gallon; e)
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0900-2023·2023-07-19

    BASIC CARE Allergy Tablets Recalled Due to Failed Quality Specifications

    BASIC CARE ALLERGY (fexofenadine hydrochloride) 180 mg tablets are being recalled nationwide due to failed impurities and product degradation specifications. Approximately 11,904 cartons were affected.

    Product
    BASIC CARE ALLERGY — BASIC CARE ALLERGY (FEXOFENADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2123-2023·2023-07-19

    Medtronic Catalyft LS Spinal Implant Recalled for Out-of-Specification Geometry

    Medtronic recalls Catalyft LS spinal implants due to potential out-of-specification dimensions. The affected devices may not properly fit or function as intended during spine fusion surgery.

    Product
    Medtronic Catalyft LS Expandable Interbody System Implant Kit, Anterior Standalone Cage, REF SPS03188, spinal implant kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0908-2023·2023-07-19

    Fexofenadine Hydrochloride Tablets Recalled for Failed Quality Specifications

    L. Perrigo is recalling 32,376 cartons of Good Sense Aller Ease antihistamine tablets nationwide due to failed quality specifications affecting impurities and degradation. Consult your healthcare provider if you have taken this product.

    Product
    GOOD SENSE ALLER EASE — GOOD SENSE ALLER EASE (FEXOFENADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2129-2023·2023-07-19

    Ortho Recalls VITROS Chemistry Calibrator Kit 20 for Analytical Bias

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Calibrator Kit 20 due to measurement bias affecting laboratory results for immunoglobulin and complement protein testing. Falsely elevated or reduced values could be reported.

    Product
    VITROS Chemistry Products Calibrator Kit 20-in vitro diagnostic use only. VITROS Chemistry Products Calibrator Kit 20- Used to calibrate the VITROS 5,1 FS/4600 Chemistry Systems and the VITROS 5600/XT 7600 Integrated Systems for the quantitative measurement of transferrin, C3, C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0922-2023·2023-07-19

    Artificial Tears Eye Drops Recalled Due to Manufacturing Facility Contamination

    Delsam Pharma's artificial tears eye drops are being recalled nationwide due to confirmed contamination linked to manufacturing facility defects. All affected lots were distributed via two distributors.

    Product
    Delsam Pharma's ARTIFICIAL TEARS (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1%, 1/2 fl oz (15 ml) bottle, Distributed By: Delsam Pharma Llc, Bronx, New York 10467, NDC 72570 121 15.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0903-2023·2023-07-19

    Allergy Relief Fexofenadine Hydrochloride Tablets Recalled for Failed Quality Specifications

    CVS Pharmacy is recalling 16,200 cartons of Allergy Relief fexofenadine hydrochloride tablets nationwide due to failed impurities and degradation specifications. Stop using affected lot 2DV1925 and consult a pharmacist.

    Product
    Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 30-count cartons, Distributed By: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895. NDC 69842-0914-39
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0920-2023·2023-07-19

    EzriCare Artificial Tears Eye Drops Recalled for Manufacturing Contamination

    EzriCare Artificial Tears eye drops are being recalled nationwide due to manufacturing facility contamination and CGMP deviations. The recall includes multiple lot numbers distributed nationwide.

    Product
    Artificial Tears (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1/2 fl oz (15 ml) bottle, Distributed by. EzriCare, LLC, Lakewood, NJ, NDC 79503-0101-15.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0914-2023·2023-07-19

    FDA Recalls Tiagabine Hydrochloride Tablets Due to Impurity Specification Failures

    Sun Pharmaceutical is recalling Tiagabine Hydrochloride Tablets (2 mg) due to out-of-specification impurities detected during testing. The recall affects lot HAC3339A distributed nationwide.

    Product
    TIAGABINE HYDROCHLORIDE — TIAGABINE HYDROCHLORIDE (TIAGABINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-07192023-01·2023-07-19

    Never Any! Ham and Cheese Lunch Kits Alerted for Undeclared Peanut

    USDA FSIS issued a public health alert for Never Any! ham and cheese lunch kits containing chocolate chip cookies that may contain undeclared peanut.

    Product
    FSIS Issues Public Health Alert for Never Any! Brand Ready-To-Eat Ham and Cheese Lunch Kits Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2119-2023·2023-07-19

    Medtronic Catalyft LS Spinal Implants Recalled for Out-of-Specification Dimensions

    Medtronic recalls 25 units of Catalyft LS spinal implants (lot numbers NM21J039, NM21M026) due to out-of-specification device dimensions that may affect surgical fit and function.

    Product
    Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981025522, spinal implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2130-2023·2023-07-19

    Ambulance stretcher base leg assembly may bend causing tip and unstable motion

    Stryker Power-PRO 2 ambulance cots may develop bent base leg assemblies, risking cot tips, unstable motion, and operational difficulties. Approximately 1,980 units were recalled.

    Product
    Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled, retractable X-frame that is designed to support and transport a maximum weight of 700 lb (318 kg). Model Number: 6507
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2128-2023·2023-07-19

    Abiomed Introducer Set Recall Due to Sidearm Detachment Risk

    Abiomed 14Fr Low Profile Introducer Sets are being recalled due to silicone oil contamination that may cause sidearm detachment during use. One detachment has been documented; no injuries have been reported.

    Product
    Abiomed 14Fr Low Profile Introducer Set, Product Number 1000457
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2138-2023·2023-07-19

    Medical Blood Cell Diluent Recalled for Out-of-Specification Parameters

    Beckman Coulter is recalling specific lots of COULTER DxH Diluent due to out-of-specification conductivity, osmolality, and pH. The diluent may produce inaccurate blood cell test results.

    Product
    COULTER DxH Diluent, REF 628017; diluent used for counting and sizing blood cells
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1235-2023·2023-07-19

    Multiple frozen berry products recalled for potential Hepatitis A contamination

    Oregon Potato Company is recalling frozen berry products distributed nationwide under multiple brand names due to potential Hepatitis A contamination. Consumers who have purchased these products should not consume them.

    Product
    Rader Farms Organic Berry Trio Strawberry, Blackberry, Raspberry. Item # 105872. Frozen, packed into flexible plastic bags. Net wt. 3lbs. UPC on retail bag: 8 84038 85143 4. A total of 6 sellable units (3lbs. each) are placed into a case for distribution to retailer. DISTRIBUTE
    Category
    Food
    Distribution
    32 states
  • HighFDA (Devices)·Z-2109-2023·2023-07-19

    Surgical chest support device recalled for potential cracking at attachment

    Baxter Healthcare recalls 1,010 Allen Advance Chest Support devices due to potential cracking where the support attaches to operating room table rails. No injuries reported.

    Product
    Allen Advance Chest Support with Pad
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0918-2023·2023-07-19

    FDA Recalls Bivalirudin Injectable Drug Due to Particulate Matter

    Accord Healthcare is recalling Bivalirudin for Injection lot M2212070 due to the presence of fiber particles. Bivalirudin is an injectable blood thinner used in cardiac procedures.

    Product
    BIVALIRUDIN — BIVALIRUDIN (BIVALIRUDIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2117-2023·2023-07-19

    Medtronic spinal implant recall due to out-of-specification device dimensions

    Medtronic Catalyft LS Expandable Interbody System spinal implants are being recalled due to out-of-specification device dimensions that may affect proper placement and spinal support.

    Product
    Medtronic Catalyft LS Expandable Interbody System, Anterier Standalone Cage, REF 981023322, spinal implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2118-2023·2023-07-19

    Medtronic Catalyft LS spinal implant recalled for out-of-specification device dimensions

    Medtronic is recalling eight units of Catalyft LS Expandable Interbody System spinal implants due to potential out-of-specification device dimensions that could affect surgical fitting and spinal stability.

    Product
    Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981023325, spinal implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0902-2023·2023-07-19

    Careone Allergy Relief tablets recalled for failed impurity and degradation specifications

    Careone Allergy Relief fexofenadine hydrochloride 180mg tablets are recalled nationwide for failing impurity and degradation specifications. Lot 2JE2185 with expiration date 01/24 is affected.

    Product
    CAREONE ALLERGY RELIEF — CAREONE ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2107-2023·2023-07-19

    Orthopedic Screw Recall Due to Undersized Head in Surgical Device

    Osteomed is recalling orthopedic screws with undersized heads that may pass through bone plates. Affected lot numbers were distributed nationwide in the US and Singapore.

    Product
    REF: 218-1604, 1.6mm x 4mm Profile Zero Auto-Drive Screw, Rx Only, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1246-2023·2023-07-19

    Protein supplement powder recalled for potential Staphylococcus aureus contamination

    1st Phorm Level-1 protein supplement (Chocolate Marshmallow) is recalled because it may contain Staphylococcus aureus, a bacterium that can cause serious foodborne illness.

    Product
    1st phorm Level-1 Sustained Assimilation Protein. Chocolate Marshmallow. Protein Supplement. Item number 502396. Net Wt. 2.45 lbs (1.11kg) UPC 8 50036-64808 6. Manufactured & Designed Exclusively for 1st Phorm, 2091 Fenton Logistics Pk Blvd, Fenton, MO 63026
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2127-2023·2023-07-19

    GE Vivid S70N Ultrasound Device Boot Failure Recall

    GE Healthcare recalls certain Vivid S70N ultrasound devices that may not boot promptly, potentially delaying availability in time-critical emergencies.

    Product
    GE Healthcare Vivid S70N, ultrasound device
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·23V499000·2023-07-19

    Ford Transit Vans Recalled for Fuel Hose Fire Risk

    Quality Vans is recalling 2020-2023 Ford Transit vans with specific generators because a fuel hose may not be secured, posing a fire risk.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2122-2023·2023-07-19

    Medtronic Catalyft LS Spinal Implant Recall for Out-of-Spec Geometry

    Medtronic is recalling Catalyft LS spinal implants due to potential out-of-specification device geometries that may not properly accommodate patient anatomy.

    Product
    Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981027725, spinal implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0901-2023·2023-07-19

    Berkley Jensen Allergy Relief Recalled for Failed Quality Specifications

    L. Perrigo Company is recalling Berkley Jensen Allergy Relief tablets due to failed product quality specifications involving impurities and degradation. Consumers should verify their lot numbers and expiration dates.

    Product
    BERKLEY JENSEN ALLERGY RELIEF — BERKLEY JENSEN ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0913-2023·2023-07-19

    Sunitinib Malate Capsules Recalled Due to Excess Moisture Content

    Teva Pharmaceuticals is recalling 180 bottles of Sunitinib Malate Capsules due to moisture content exceeding approved specifications. The affected lot (100037220) expires 10/2024.

    Product
    SUNITINIB MALATE — SUNITINIB MALATE (SUNITINIB MALATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2126-2023·2023-07-19

    GE Healthcare Vivid S60N ultrasound devices experience boot-up delays

    GE Healthcare Vivid S60N ultrasound systems may fail to boot in a timely manner. This can delay device availability during time-critical emergency situations.

    Product
    GE Healthcare Vivid S60N, ultrasound device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2136-2023·2023-07-19

    Medline Non-Sterile PVP Solution Mislabeled as Sterile in Ophthalmic Kits

    Medline Industries is recalling 1,500 units of non-sterile PVP solution mislabeled as sterile in ophthalmic and eye surgical kits. Users may unknowingly apply non-sterile solution in eye procedures, risking infection.

    Product
    MEDLINE NON-STERILE PVP SOLUTION, packaged in kits as follows: a) OCULOPLASTY PACK, Model Number DYNJ64572A; b) EYE PACK, Model Number VAL050EEPKB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2143-2023·2023-07-19

    HeartSine Defibrillator Battery and Electrode Cartridges May Fail to Function

    HeartSine battery and electrode cartridges for defibrillators may contain depleted battery cells, rendering them inoperable and preventing cardiac rhythm analysis or therapy delivery. Approximately 30,022 units are affected worldwide.

    Product
    HeartSine, REF: PAD-PAK-01, PAD-PAK-03 AND PAD-PAK-03j, CE0123 sold separately and with the HeartSine Samaritan Public Access Defibrillator models: 350P/360P/450P/500P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2125-2023·2023-07-19

    GE Healthcare Vivid S70 ultrasound systems fail to boot timely

    GE Healthcare Vivid S70 ultrasound devices may experience delayed startup. This can reduce equipment availability during time-critical emergency situations.

    Product
    GE Healthcare Vivid S70, ultrasound device
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2120-2023·2023-07-19

    Medtronic Catalyft LS Spinal Implants Recalled for Out-of-Specification Geometry

    Medtronic is recalling 11 units of its Catalyft LS Expandable Interbody System spinal implants due to potential out-of-specification dimensions that could affect surgical fit and stability.

    Product
    Medtronic Catalyft LS Expandable Interbody System, Anterior Standalone Cage, REF 981025525, spinal implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2137-2023·2023-07-19

    Medline Non-Sterile PVP Surgical Solution Kits Mislabeled as Sterile

    Medline is recalling 4,500 surgical kits because the non-sterile PVP solution inside was mislabeled as sterile. Using the mislabeled product in sterile surgical procedures could introduce non-sterile materials into surgical fields.

    Product
    MEDLINE NON-STERILE PVP SOLUTION, packaged in kits as follows: a) TOTAL JOINT, Model Number CDS985555S; b) TOTAL KNEE, Model Number CDS985566Q; c) MAJOR ORTHO-LF, Model Number DYNJ0949139I; d) BSHR TOTAL KNEE-LF, Model Number DYNJ24525K; e) BSHR TOTAL HIP-LF, Model Number DYNJ24
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1249-2023·2023-07-19

    Ranch Salad Dressing Recalled for Product Spoilage

    SCREAMING EAGLE CO PACK LLC is recalling Tony Charchere's Ranch Salad Dressing due to bubbling and sour taste indicating spoilage. No illnesses have been reported.

    Product
    Tony Charchere's Ranch Salad Dressing packaged in 12oz PET bottle - 6 bottles per case
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0912-2023·2023-07-19

    OTC Allergy Relief Tablets Recalled for Failed Manufacturing Specifications

    Topcare Allergy Relief 180 mg tablets recalled for failed impurity and degradation specifications. The recall affects 44,280 cartons distributed nationwide.

    Product
    TOPCARE ALLERGY RELIEF — TOPCARE ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0896-2023·2023-07-19

    Vivus Pancreaze prescription drug recall for failed stability specifications

    Vivus, Inc. is recalling Pancreaze delayed-release capsules nationwide due to failed stability specifications. The affected lot may not maintain product strength through the stated expiration date.

    Product
    PANCREAZE — PANCREAZE (PANCRELIPASE LIPASE, PANCRELIPASE AMYLASE, AND PANCRELIPASE PROTEASE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0898-2023·2023-07-19

    Eye drops Equate and private-label brands recalled for manufacturing documentation deficiency

    K.C. Pharmaceuticals is recalling 397,430 bottles of Equate and private-label dry eye relief drops nationwide due to Current Good Manufacturing Practice deficiencies related to fill line documentation.

    Product
    EQUATE EYE DROPS DRY EYE RELIEF — EQUATE EYE DROPS DRY EYE RELIEF (GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0899-2023·2023-07-19

    Amlodipine Besylate 10 mg Tablets Recalled for Failing Potency Tests

    Lupin Pharmaceuticals recalls Amlodipine Besylate 10 mg tablets (Lot A102887) after stability testing revealed the tablets failed potency specifications, containing less active ingredient than labeled. Patients should contact their pharmacist or doctor.

    Product
    AMLODIPINE BESYLATE — AMLODIPINE BESYLATE (AMLODIPINE BESYLATE)
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0910-2023·2023-07-19

    FDA Recalls Fexofenadine Allergy Relief Tablets Due to Impurity and Degradation Issues

    Target's store-brand fexofenadine allergy relief tablets are being recalled nationwide due to failed quality specifications for impurities and degradation. Consumers should stop using affected lots and contact Target or their healthcare provider.

    Product
    allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-count cartons (NDC 11673-617-22), b)30-count cartons (NDC 11673-617-39), c)70-count cartons (NDC 11673-617-01), and d)150-count cartons (11673-617-47), Distributed by: Target Corporation, Minneapolis, MN
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2132-2023·2023-07-19

    Medline Non-Sterile PVP Solution Mislabeled as Sterile Product

    Medline Industries recalled 15 units of non-sterile PVP solution in EAR CDS kits that were mislabeled as 'Sterile PVP SLN' instead of 'Non-Sterile PVP Solution, Sterile Packaging.' The mislabeling could result in inappropriate use in sterile medical applications.

    Product
    MEDLINE NON-STERILE PVP SOLUTION, packaged in kits as follows: EAR CDS, Model Number CDS980089O
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0904-2023·2023-07-19

    OTC Antihistamine Tablets Recalled for Failed Quality Specifications

    L. Perrigo Company is recalling 1,920 cartons of Exchange Select Aller Ease (Fexofenadine Hydrochloride) 180 mg tablets nationwide due to failed impurity and degradation specifications.

    Product
    EXCHANGE SELECT ALLER EASE — EXCHANGE SELECT ALLER EASE (FEXOFENADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0906-2023·2023-07-19

    OTC Allergy Relief Medication Recalled for Failed Quality Specifications

    L. Perrigo Company is recalling approximately 59,688 cartons of Fexofenadine Hydrochloride 180 mg allergy relief tablets nationwide because the product failed to meet FDA specifications for impurities and degradation.

    Product
    ALLERGY RELIEF — ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1237-2023·2023-07-19

    Coca-Cola bottler recalls incorrectly labeled zero-sugar beverages in Georgia

    Coca Cola Bottling Group United is recalling 177 cases of Coca-Cola Ultimate in Georgia because products labeled as 'Zero Sugar' actually contain regular sugar. The mislabeling affects consumers monitoring their sugar intake.

    Product
    Coca Cola Ultimate; packaged in 20oz PET bottles, 24 loose bottles per case *Product incorrectly labeled as Coca Cola Ultimate Zero Sugar
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0905-2023·2023-07-19

    Kirkland Signature Aller Fex Allergy Tablets Recalled for Failed Impurities Specifications

    L. Perrigo Company recalls Kirkland Signature Aller Fex allergy tablets nationwide due to certain lots failing impurities and degradation quality specifications. Consumers with affected lots should contact their healthcare provider.

    Product
    KIRKLAND SIGNATURE ALLER FEX — KIRKLAND SIGNATURE ALLER FEX (FEXOFENADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E055000·2023-07-18

    Cummins Recalls L9 Diesel Engines Due to Fuel Hose Defect

    Cummins is recalling specific L9 Diesel Engines because damaged fuel filter hoses may leak or disconnect, increasing the risk of engine stall or fire.

    Product
    FUEL SYSTEM, DIESEL:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E054000·2023-07-18

    Cummins Recalls B6.7 Diesel Engines Due to Lifting Bracket Bolt Issue

    Cummins is recalling certain B6.7 diesel engines because an insufficiently tightened bolt may cause the rear lifting bracket to detach, increasing injury risk during lifting.

    Product
    ENGINE AND ENGINE COOLING:ENGINE:DIESEL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V495000·2023-07-18

    Titan Bus Recalls 2017-2021 Models for Missing Mirror Warning Label

    Titan Bus is recalling 2017-2021 SRW and DRW school buses because a warning label may be missing from the Cross View Mirror, potentially increasing crash risk.

    Product
    TITAN BUS — TITAN BUS SRW, DRW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V496000·2023-07-18

    2021 Nissan Kicks vehicles recalled for power steering defect

    Nissan is recalling 2021 Kicks vehicles due to an intermittent electrical connection in the power steering system that can disable power steering assist. Loss of power steering increases steering effort and crash risk.

    Product
    NISSAN — NISSAN KICKS, VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V492000·2023-07-17

    Kidron Refrigerated Trailers Recalled for Tire Pressure Loss Risk

    STE Hackney is recalling 2022-2023 Kidron refrigerated trailers because tire pressure may drop at speeds over 45 mph, increasing crash risk.

    Product
    KIDRON — KIDRON REFRIGERATED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V491000·2023-07-17

    Maxvan Pathway and Route Recalled for Fuel Hose Leak Risk

    Adaptive Mobility Systems is recalling 2020-2023 Maxvan Pathway and 2021 Route vehicles because a fuel hose may leak gasoline, increasing fire risk.

    Product
    MAXVAN — MAXVAN PATHWAY, ROUTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V490000·2023-07-17

    Grand Design RV Recall: Improperly Tightened Suspension U-Bolts

    Grand Design is recalling certain 2021–2024 Solitude and Momentum fifth wheels with improperly tightened suspension U-bolts. Loose U-bolts can cause the axle to move, leading to loss of vehicle control.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM, SOLITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V494000·2023-07-17

    2018-2023 Nissan Leaf vehicles recalled for unintentional acceleration risk

    Nissan is recalling certain 2018-2023 Leaf vehicles that may accelerate unintentionally when the driving mode is changed after disengaging cruise control. The defect increases the risk of crashes.

    Product
    NISSAN — NISSAN LEAF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V493000·2023-07-17

    Pleasure Way motorhomes recalled for fuel hose fire risk

    Pleasure Way is recalling certain 2021-2023 OnTour and Lexor motorhomes due to fuel hose defects that may cause gasoline leaks and fire risk. Dealers will inspect and replace fuel hoses free of charge.

    Product
    PLEASURE WAY — PLEASURE WAY ONTOUR, LEXOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·031-2023·2023-07-15

    Mulan Dumpling Recalls Frozen Meat and Poultry Products Produced Without Inspection

    Mulan Dumpling, LLC is recalling approximately 22,874 pounds of frozen meat and poultry dumplings produced without federal inspection. The products were distributed nationwide.

    Product
    Mulan Dumpling, LLC, Recalls Frozen Meat and Poultry Dumpling Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·030-2023·2023-07-14

    Suya Slice LLC Recalls Ready-to-Eat Beef Products Produced Without Inspection

    Suya Slice LLC is recalling approximately 445 pounds of ready-to-eat beef products because they were produced without federal inspection.

    Product
    Suya Slice LLC, Recalls Ready-to-Eat Beef Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V484000·2023-07-14

    McLaren Recalls 600LT Vehicles Due to Coolant Leak Fire Risk

    McLaren is recalling 2019-2020 600LT vehicles because a coolant leak could cause a fire. Dealers will replace the affected hose and housing free of charge.

    Product
    MCLAREN — MCLAREN 600LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V487000·2023-07-14

    Mazda recalls 2014-2018 Mazda3 and CX-3 for faulty rearview cameras

    Mazda is recalling 2014-2018 Mazda3 and 2016-2021 CX-3 vehicles because rearview cameras may display flickering or distorted images, reducing visibility and increasing crash risk. Dealers will inspect and replace cameras free of charge.

    Product
    MAZDA — MAZDA MAZDA3, CX-3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V486000·2023-07-14

    Motorhomes: Overheating HVAC Wiring Could Cause Fires in Entegra, Jayco Models

    Certain 2020-2021 Entegra and Jayco motorhomes are recalled because inadequate HVAC blower motor circuit wiring can overheat, increasing fire risk. The remedy involves relocating and replacing the fuse and wiring harness.

    Product
    ENTEGRA — ENTEGRA, JAYCO LAUNCH, MELBOURNE PRESTIGE, MELBOURNE, QWEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V489000·2023-07-14

    Tesla Recalls 2023 Model S, X, and Y for Camera Misalignment

    Tesla is recalling 2023 Model S, X, and Y vehicles because a misaligned forward-facing camera may disable active safety features without warning, increasing crash risk.

    Product
    TESLA — TESLA MODEL Y, MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V488000·2023-07-14

    Tesla Model S and Model X seat belts may detach in crash

    Tesla is recalling certain 2021-2023 Model S and Model X vehicles because front-row seat belts may not be connected properly to pretensioner anchors and could detach. A detached seat belt may fail to properly restrain an occupant during a crash.

    Product
    TESLA — TESLA MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23244·2023-07-13

    Frigidaire Gas Laundry Centers Recalled Due to Fire Hazard

    Electrolux Group is recalling about 13,600 Frigidaire Gas Laundry Centers because the felt seal on the dryer drum can fold inward, causing lint to accumulate and creating a fire hazard. The company has received 23 reports of fire and one report of smoke inhalation injury.

    Product
    Frigidaire Gas Laundry Centers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23773·2023-07-13

    Yamaha Personal Transportation Vehicles Recalled for Unexpected Acceleration Hazard

    Yamaha is recalling approximately 370 personal transportation vehicles sold nationwide from August 2022 through March 2023 because they can accelerate unexpectedly, creating crash and injury hazards.

    Product
    Yamaha Personal Transportation Vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23243·2023-07-13

    Gas-Fired Residential Boilers Recalled for Carbon Monoxide Exposure Risk

    ECR International is recalling about 1,745 gas-fired hot water residential boilers that may be missing a flue inspection cover plate, which can expose residents to combustion flue gases and carbon monoxide poisoning.

    Product
    Gas-fired hot water residential boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1038-2023·2023-07-12

    Seasoned Flour Recalled Due to Potential Salmonella Contamination

    Newly Weds Foods is recalling A52541 seasoned flour (product code MT110322C) due to potential Salmonella contamination. The product has been distributed across the United States and Canada.

    Product
    A52541 SEASONED FLOUR X1 50.00 BAG
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·F-1145-2023·2023-07-12

    Meatball Seasoning Recalled Due to Potential Salmonella Contamination

    Newly Weds Foods is recalling G60040 Meatball Seasoning due to potential Salmonella contamination. The product was distributed across 28 U.S. states and Canada.

    Product
    G60040 MEATBALL SEASONING X1 50.00 BAG
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·F-1212-2023·2023-07-12

    Lemon Garlic Seasoning for Chicken Recalled for Salmonella Contamination Risk

    Newly Weds Foods is recalling Lemon Garlic Seasoning for Chicken (code SE280822) due to potential Salmonella contamination. The product was distributed across 28 US states and Canada.

    Product
    S16997 LEMON GARLIC SEASONING FOR CHICKEN P1 50.00 BOX
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·F-1194-2023·2023-07-12

    BBQ Seasoning Recalled Due to Possible Salmonella Contamination

    Newly Weds Foods is recalling Chix BBQ Seasoning due to possible Salmonella contamination. The product was distributed to 28 US states and Canada.

    Product
    S02192 CHIX BBQ SEASONING X1 52.72 BAG
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·F-1040-2023·2023-07-12

    Breader Product Recall Due to Possible Salmonella Contamination

    Newly Weds Foods, Inc. is recalling A54518 Breader products because they may contain Salmonella. The recall affects products distributed across multiple U.S. states and Canada.

    Product
    A54518 BREADER X1 50.00 BAG
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·F-1155-2023·2023-07-12

    Meatloaf Seasoning Recalled Due to Potential Salmonella Contamination

    Newly Weds Foods is recalling G76099 Meatloaf Seasoning due to potential Salmonella contamination. The affected product was distributed across 28 states and Canada.

    Product
    G76099 MEATLOAF SEASONING X3 42.00 BAG
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·F-1200-2023·2023-07-12

    Savory Marinade Recalled Due to Potential Salmonella Contamination

    Newly Weds Foods is recalling savory marinade products that may contain Salmonella. The recall affects products distributed to 27 US states and Canada.

    Product
    S08824 SAVORY MARINADE X1 50.00 BAG
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Food)·F-1202-2023·2023-07-12

    Newly Weds Foods ADNE-ARC Blend Recalled Due to Salmonella Risk

    Newly Weds Foods is recalling its ADNE-ARC Blend due to possible Salmonella contamination. The product was distributed across multiple US states and Canada.

    Product
    S09557 ADNE-ARC BLEND X1 36.00 BAG
    Category
    Food
    Distribution
    28 states

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