The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

22076–22100 of 114376

  • 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 (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 (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-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 (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-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 (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 (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 (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 (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 (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…
    Category
    Food
    Distribution
    6 states
  • 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-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-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
  • 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-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 (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-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-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
  • 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…
    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 (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