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.

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Category

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Minimum severity

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

Clear filters

25026–25050 of 90141

  • SevereFDA (Food)·F-1283-2022·2022-06-15

    Taharka Brothers Peanut Butter Cup Ice Cream Recalled for Salmonella

    Taharka Brothers Peanut Butter Cup Ice Cream sold in Maryland, Virginia, and Washington D.C. is being recalled due to potential Salmonella contamination. Consumers should discard the product.

    Product
    Taharka Brothers Peanut Butter Cup Ice Cream 16 oz Pint Container: Paper cup with peanut butter cups along the bottom with a white background. Barcode: 38455-78827 2.5 Gallon: Brown and rectangular cardboard container with a white sticker label
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1192-2022·2022-06-15

    Chocolate Candy Recalled Nationwide for Potential Salmonella

    ELITE EXTRA CREAMY MILK CHOCOLATE WITH VANILLA & COOKIES is recalled nationwide due to potential Salmonella contamination affecting all lots.

    Product
    ELITE EXTRA CREAMY MILK CHOCOLATE WITH VANILLA & COOKIES UPC:815871012294 Net Wt. 3.35oz (100g). Red packaging.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1261-2022·2022-06-15

    Keats London Vegan Irish Cream Truffles Recalled for Undeclared Milk

    Keats London Vegan Irish Cream Truffles may contain undeclared milk. Consumers with milk allergies should not consume this product and should discard it.

    Product
    Keats London Vegan Irish Cream Truffles in a 4.93-ounce round blue plastic package.
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1190-2022·2022-06-15

    Elite White Chocolate with Cookie Pieces Recalled for Salmonella Risk

    Elite Confectionery Ltd is recalling Elite White Chocolate with Cookie Pieces (UPC: 815871015707) nationwide due to potential Salmonella contamination. All lot codes are affected.

    Product
    ELITE WHITE CHOCOLATE WITH COOKIE PIECES UPC: 815871015707 Net Wt. 3.53 oz (100g). Red packaging.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1168-2022·2022-06-15

    FDA Recalls Compounded Tacrolimus Suspension Due to Subpotency

    Valor Compounding Pharmacy issued a Class I recall for compounded Tacrolimus suspension (Lot 04272022@35) distributed in California due to subpotency.

    Product
    Tacrolimus (Brand Capsules ) 0.5 mg/mL Suspension, Rx, This is a compounded medication., Valor Compounding Pharmacy, 2461 Shattuck Ave., Berkeley, CA 94704
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1247-2022·2022-06-15

    Elite Refreshing Mint Chewing Gum Recalled for Potential Salmonella Contamination

    Elite Refreshing Mint Flavored Chewing Gum has been recalled due to potential Salmonella contamination. The FDA Class I recall affects all lots distributed nationwide.

    Product
    ELITE REFRESHING MINT FLAVORED CHEWING GUM UPC:815871014632 NET WT. 2.32oz (66 g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1246-2022·2022-06-15

    Elite Spearmint Chewing Gum Recalled Due to Salmonella Contamination Risk

    Elite Spearmint Flavored Chewing Gum is recalled nationwide due to potential Salmonella contamination affecting all lot numbers.

    Product
    ELITE SPEARMINT FLAVORED CHEWING GUM UPC:815871014625 NET WT. 2.32oz (66 g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1160-2022·2022-06-15

    Diced Potatoes from Carol's Cuts Recalled for Undeclared Sodium Metabisulfite

    Liberty Fruit Co Inc (Carol's Cuts) is recalling diced potatoes because sodium metabisulfite is not declared on the product label. The undeclared ingredient can cause allergic reactions in people with sulfite sensitivity.

    Product
    POTATO YUKON DICED 4/5# C/C (01)10886810715337(10)0016086768 71533 Best if used by: 04/25/22, 04/28/22 Ingredients: Potato, Sodium Metabisulfite
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-1167-2022·2022-06-15

    Tacrolimus Compounded Suspension Recalled Due to Subpotency

    Valor Compounding Pharmacy recalls compounded Tacrolimus 0.5 mg/mL suspension due to subpotency. The medication, distributed in California, may not provide adequate therapeutic levels for immunosuppression in transplant patients.

    Product
    Tacrolimus (Brand Capsules ) 0.5 mg/mL Suspension, Rx, This is a compounded medication., Valor Compounding Pharmacy, 2461 Shattuck Ave., Berkeley, CA 94704,
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1259-2022·2022-06-15

    Vegan Hazelnut Truffles Recalled for Undeclared Milk Allergen

    The FDA is recalling Pimlico Confectioners Vegan Fine Hazelnut Truffles because they may contain undeclared milk. Consumers with milk allergies should not eat this product.

    Product
    Pimlico Confectioners Vegan Fine Hazelnut Truffles in a 3.88-ounce green plastic package.
    Category
    Food
    Distribution
    49 states
  • SevereFDA (Food)·F-1170-2022·2022-06-15

    Frozen Yukon Potatoes Recalled for Undeclared Ingredient

    Liberty Fruit Co Inc is recalling frozen Yukon "A" Dice potatoes because sodium metabisulfite was not declared on the product label. The product was distributed to food service locations in Kansas, Nebraska, Iowa, and Missouri.

    Product
    POT. YUKON "A" DICE/SK 25# CC (01)10886810715368(10)0016088728 71536 Best if used by: 04/12/22, 04/14/22, 04/19/22 Ingredients: Potato, Sodium Metabisulfite
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1198-2022·2022-06-15

    Elite Blondy chocolate confectionery recalled for potential Salmonella contamination

    Elite Blondy with Hazelnut Cream (UPC 815871015011) is being recalled nationwide due to potential Salmonella contamination. All lots are included in the recall.

    Product
    ELITE BLONDY WITH HAZELNUT CREAM UPC: 815871015011 Net Wt. 3.53oz (100g).Yellow packaging
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1088-2022·2022-06-15

    Levofloxacin 500 mg Tablets Recalled Due to Manufacturing Temperature Abuse

    Mckesson Medical-Surgical is recalling Levofloxacin 500 mg tablets nationwide due to temperature abuse during manufacturing that violated pharmaceutical quality standards.

    Product
    LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0996-2022·2022-06-15

    Topex Benzocaine Topical Anesthetic Recalled for Temperature-Abuse Manufacturing Deviation

    McKesson Medical-Surgical is recalling Topex benzocaine 20% topical anesthetic gel due to cGMP deviations involving temperature abuse during manufacturing. The recall affects 24 bottles distributed nationwide.

    Product
    Topex (benzocaine 20%), Topical Anesthetic Gel Strawberry, 1 oz, Rx only, Manufacturer: DS Healthcare, NDC 0699-5116-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0991-2022·2022-06-15

    Walgreens Earache Drops recalled for microbial contamination of non-sterile product

    Walgreens Earache Drops are recalled due to microbial contamination in the non-sterile product. Consumers should stop using the product and consult a healthcare provider if they experience any adverse effects.

    Product
    WALGREENS EARACHE DROPS — WALGREENS EARACHE DROPS (BELLADONNA LEAF, CALCIUM CARBONATE, CHAMOMILE, LYCOPODIUM CLAVATUM SPORE, ANEMONE PATENS, AND SULFUR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1110-2022·2022-06-15

    FDA Recalls Metoprolol Tablets Due to Temperature Abuse During Manufacturing

    McKesson Medical-Surgical is recalling Metoprolol 50 mg tablets nationwide due to temperature abuse during manufacturing that may compromise medication stability. Patients should contact their pharmacist or physician.

    Product
    Metoprolol tablets 50 mg, 100-count botte, Rx only, MFG: Sun Pharmaceuticals, NDC 57664-0477-52
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1246-2022·2022-06-15

    Siemens Artis Icono Angiography Systems Pose Electric Shock Risk

    Siemens Artis icono angiography systems may pose electric shock risk if protective grounding is interrupted. Affected units sold nationwide; users should verify equipment grounding integrity.

    Product
    Artis icono floor-angiography systems developed for single and biplane diagnostic imaging and interventional procedures SMN: 11327700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1026-2022·2022-06-15

    Apraclonidine ophthalmic solution recalled for temperature-abuse manufacturing defect

    McKesson Medical-Surgical is recalling 21 bottles of Apraclonidine 0.5% ophthalmic solution due to cGMP deviations involving temperature abuse during manufacturing. The temperature exposure may reduce drug efficacy.

    Product
    APRACLONIDINE — APRACLONIDINE (APRACLONIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1300-2022·2022-06-15

    Frigo Mozzarella Cheese recalled for undeclared milk allergen

    Frigo Low Moisture Mozzarella Cheese is being recalled because milk is not declared on the label. Consumers with milk allergies may be affected.

    Product
    Frigo Part-Skim Low Moisture Part Skim Mozzarella Cheese Net Wt. 2lb. (907g) Saputo Cheese USA, Inc. Lincolnshire, IL 60069 UPC: 041716131138
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-1035-2022·2022-06-15

    Ophthalmic Drug Isopto Atropine Recalled Due to Manufacturing Temperature Deviation

    McKesson Medical-Surgical is recalling 13 bottles of Isopto Atropine 1% ophthalmic solution due to temperature-abuse violations of manufacturing standards that may have affected product sterility.

    Product
    ISOPTO ATROPINE — ISOPTO ATROPINE (ATROPINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1245-2022·2022-06-15

    Siemens Artis icono Angiography Systems: Risk of Electric Shock from Grounding Failure

    Siemens is recalling 51 Artis icono biplane angiography systems due to a potential grounding failure that could allow electric shock if someone contacts metallic parts during use.

    Product
    Artis icono biplane -angiography systems developed for single and biplane diagnostic imaging and interventional procedures SMN: 11327600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1254-2022·2022-06-15

    MedMinder Medication Dispenser Emergency Alert Function No Longer Operational

    MedMinder Medication Dispensers will no longer connect to the emergency alert system for all models. The device's emergency communication capability has been discontinued for approximately 2,701 units nationwide.

    Product
    MedMinder Medication Dispenser- Intended to serve as a medication reminder to promote medication adherence with additional feature to communicate with emergency call center.
    Category
    Medical Device
    Distribution
    Distributed nationwide