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 deaths or serious injuries are reported, 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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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)

Clear filters

2576–2600 of 11819

  • HighFDA (Drugs)·D-1142-2022·2022-06-22

    Alcohol Antiseptic Hand Sanitizer Recalled for Chemical Contamination

    A.P. Nonweiler is recalling its 80% alcohol antiseptic hand sanitizer because FDA testing found acetaldehyde and acetal above safe specification limits. The product was distributed in Wisconsin and Virginia.

    Product
    Alcohol Antiseptic 80%, Topical Solution, Hand Sanitizer, Non-Sterile Solution, Packaged as (a) 250 U.S. gallons per tote, Product Code 9999D361-250: (b) 1 U.S. gallon, Product Code 9999D361-001: A.P. Nonweiler Co., Inc., 3321 County Road A, Oshkosh, WI 54901.
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Drugs)·D-1143-2022·2022-06-22

    Prefilled Syringes of Medroxyprogesterone Acetate Recalled for Lack of Sterility Assurance

    Afaxys Pharma is recalling 79,339 prefilled syringes of medroxyprogesterone acetate because the manufacturer could not assure sterility. The syringes were distributed nationwide.

    Product
    medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured by: Sun Pharmaceutical Industries, Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India Distributed by: Afaxys Pharma, LLC, Charleston, SC, 29403, USA, Product of
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1147-2022·2022-06-22

    Medroxyprogesterone acetate injectable vials recalled for lack of sterility assurance

    Sun Pharmaceutical is recalling 26,892 vials of medroxyprogesterone acetate injectable suspension (150 mg/mL) distributed nationwide due to lack of assurance of sterility. The affected lots expire between January and June 2023.

    Product
    medroxyPROGESTERone Acetate Injectable Suspension, USP, 25 x 1 mL Single-Dose Vial, 150 mg/mL, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol Baroda Highway, Halol-389 350, Gujarat India
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1126-2022·2022-06-22

    Homeopathic drug Bacillinum Pulmo recalled for manufacturing deviations

    Washington Homeopathic Products recalled Bacillinum Pulmo homeopathic drug due to manufacturing practice deviations. The Class II recall, initiated in May 2022 and terminated in May 2023, affected nationwide distribution.

    Product
    Bacillinum Pulmo, Potency: 30C, 200C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1149-2022·2022-06-22

    Hand Sanitizer Recalled for Acetaldehyde and Acetal Above Limits

    Hand Sanitizer LLC is recalling Say Goodbye to Germs hand sanitizer bottles due to CGMP deviations. FDA testing found acetaldehyde and acetal levels above acceptable limits.

    Product
    HAND SANITIZER SAY GOODBYE TO GERMS Alcohol Antiseptic 80% Topical Non-Sterile Solution, 12 FL OZ (254 mL) bottles, Distributed by: Hand Cleansing Gel 850 Kaliste Saloom Rd. Suite 212 Lafayette, LA 70508 UPC 8 60003 62626 9
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Drugs)·D-1150-2022·2022-06-22

    Zileuton Extended-Release Tablets recalled for failed dissolution specifications

    Lupin Pharmaceuticals is recalling Zileuton Extended-Release Tablets, 600 mg, due to failed dissolution specifications found during stability testing that may affect medication efficacy.

    Product
    Zileuton Extended-Release Tablets, 600 mg, 120-count bottle, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD 21202 by Lupin Limited, Nagpur-441108, India, NDC 68180-169-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1145-2022·2022-06-22

    Medroxyprogesterone Acetate Injectable Suspension Recalled for Sterility Concerns

    Sun Pharmaceutical is recalling 4,625 syringes of Medroxyprogesterone Acetate Injectable Suspension (Lot HAC1951A) due to lack of assurance of sterility. The affected medication was distributed nationwide.

    Product
    MEDROXYPROGESTERONE ACETATE — MEDROXYPROGESTERONE ACETATE (MEDROXYPROGESTERONE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1144-2022·2022-06-22

    Medroxyprogesterone Acetate Injectable Suspension Recalled for Sterility Assurance Failure

    Sun Pharmaceutical is recalling medroxyprogesterone acetate injectable suspension due to lack of assurance of sterility. The recall affects approximately 57,997 prefilled syringes distributed nationwide.

    Product
    medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 16714-999-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22161·2022-06-16

    Walgreens Acetaminophen Bottles Recalled for Non-Compliant Packaging

    Aurohealth recalled Walgreens brand acetaminophen 500 mg bottles (150 count) because the packaging does not meet child-resistant requirements under the Poison Prevention Packaging Act, posing a poisoning risk to young children.

    Product
    Walgreens Pain Reliever Acetaminophen, 150 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22162·2022-06-16

    Kroger Acetaminophen Recalled for Non-Child-Resistant Packaging

    Sun Pharmaceutical is recalling Kroger brand acetaminophen 650 mg extended-release caplets because the packaging does not meet child-resistant requirements under the Poison Prevention Packaging Act, posing a risk of poisoning if swallowed by young children.

    Product
    Kroger Acetaminophen, 100 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22164·2022-06-16

    Kroger Arthritis Pain Acetaminophen Recalled for Non-Child-Resistant Packaging

    Kroger-brand acetaminophen tablets in 225-count bottles lack required child-resistant packaging, posing a poisoning risk to young children if ingested. About 25,660 units were sold nationwide from December 2021 through March 2022.

    Product
    Kroger Arthritis Pain Acetaminophen, 225 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22160·2022-06-16

    Kroger Aspirin and Ibuprofen Recalled for Lack of Child-Resistant Packaging

    Time-Cap Labs is recalling Kroger-brand aspirin and ibuprofen products because the bottles lack child-resistant packaging required by law, posing a poisoning risk to young children who may swallow the contents.

    Product
    Kroger Aspirin, 300 count bottles and Ibuprofen, 160 count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • 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 (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
  • 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 (Drugs)·D-1086-2022·2022-06-15

    Gastrografin Prescription Contrast Agent Recalled for Temperature Deviations

    McKesson Medical-Surgical is recalling Gastrografin, a prescription diagnostic contrast agent, due to temperature abuse during manufacturing and distribution. The FDA classified this as a Class II recall.

    Product
    GASTROGRAFIN — GASTROGRAFIN (DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0990-2022·2022-06-15

    Homeopathic EarAche Ear Drops Recalled for Microbial Contamination

    CVS Pharmacy is recalling Homeopathic EarAche Ear Drops (lot #G11639, exp. 09/24) due to microbial contamination detected in the non-sterile product. Consumers should stop using affected bottles.

    Product
    Homeopathic EarAche Ear Drops, 0.33 FL OZ (10 mL) bottles, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895. NDC 59779-568-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1061-2022·2022-06-15

    FDA Recalls Methylprednisolone Acetate Injection for Temperature Abuse During Distribution

    McKesson Medical-Surgical is recalling 885 vials of Methylprednisolone Acetate Injectable Suspension USP (40 mg/mL) due to cGMP deviations from temperature abuse. The product was distributed nationwide, but specific lot numbers could not be identified by the distributor.

    Product
    MethyLPREDNISolone Acetate Injectable Suspension USP, 40 mg/mL, packaged in a) single dose vial (NDC 6714-088-01) b) 25-count box (NDC16714-088-25), Rx only, MFG: NorthstarRx/Teva Pharma USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1017-2022·2022-06-15

    GlucaGen Glucagon Injection Recalled for Temperature Control Deviations

    GlucaGen (glucagon) injection vials are being recalled due to temperature abuse during manufacturing that may have compromised product stability. The 187 vials were distributed nationwide.

    Product
    GlucaGen (glucagon) for injection, 1 mg per vial, single dose kit, Rx only, Manufactured for: Boehringer Mannheim, NDC 0597-0260-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0989-2022·2022-06-15

    Homeopathic Ear Drops Recalled Due to Microbial Contamination Risk

    EAR CARE EARACHE DROPS are being recalled nationwide due to potential microbial contamination. Rite Aid is recalling 16,374 bottles of the homeopathic otic product.

    Product
    EAR CARE EARACHE DROPS — EAR CARE EARACHE DROPS (ATROPA BELLADONNA, ANEMONE PULSATILLA, LYCOPODIUM CLAVATUM SPORE, MATRICARIA CHAMOMILLA, AND SULFUR)
    Category
    Drug
    Distribution
    Distributed nationwide