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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6476–6500 of 17974

  • ModerateFDA (Drugs)·D-0831-2020·2020-02-12

    Teva Recalls Desmopressin Acetate Tablets Due to Missing Desiccant

    Teva Pharmaceuticals USA is recalling Desmopressin Acetate Tablets because bottles may be missing desiccant, a GMP deviation.

    Product
    Desmopressin Acetate Tablets, 0.2 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories, Inc. Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc. Parisppany, NJ 07054 USA, NDC 0591-2465-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0838-2020·2020-02-12

    Macleods Pharma Recalls Subpotent Pioglitazone and Metformin Tablets

    Macleods Pharma USA is recalling two lots of Pioglitazone and Metformin Hydrochloride tablets because they tested below the required potency levels.

    Product
    PIOGLITAZONE AND METFORMIN HYDROCHLORIDE — PIOGLITAZONE AND METFORMIN HYDROCHLORIDE (PIOGLITAZONE AND METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0827-2020·2020-02-12

    Ascend Recalls Minocycline Hydrochloride Tablets for Dissolution Failures

    Ascend Laboratories is recalling Minocycline Hydrochloride Extended-Release Tablets due to low dissolution test results.

    Product
    MINOCYCLINE HYDROCHLORIDE — MINOCYCLINE HYDROCHLORIDE (MINOCYCLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0832-2020·2020-02-12

    Graviti Pharmaceuticals Recalls Atorvastatin Calcium Tablets Due to Foreign Tablet Presence

    Graviti Pharmaceuticals is recalling 29,056 bottles of 10 mg Atorvastatin Calcium Tablets because a 20 mg tablet was found in a bottle labeled for 10 mg tablets.

    Product
    Atorvastatin Calcium Tablets, USP, 10 mg*, 90-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ 08830-3009 USA; Manufactured By: Graviti Pharmaceuticals Pvt. Ltd., Telangana -502307, INDIA; NDC 70377-027-11.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0829-2020·2020-02-12

    Unichem Recalls Clonidine Hydrochloride Tablets Due to Benzophenone Migration

    Unichem Pharmaceuticals is recalling Clonidine Hydrochloride tablets due to potential benzophenone migration from container labels. This is a precautionary measure.

    Product
    CLONIDINE HYDROCHLORIDE — CLONIDINE HYDROCHLORIDE (CLONIDINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0822-2020·2020-02-05

    Walgreens Acne Cleansing Bar Recalled for Metal Contaminant

    Shandex Personal Care Manufacturing Inc. is recalling Walgreens Acne Cleansing Bar due to the presence of a visible metal contaminant.

    Product
    Walgreens Acne Cleansing Bar, Benzoyl Peroxide 10%, NET WT 4 oz (113 g), 1 bar per carton, Distributed By: Walgreen Co., 200 Wilmot Road, Deerfield, IL 60015, NDC: 0363-0137-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0814-2020·2020-02-05

    Sildenafil 200 mg Troche Recall for Labeling and Expiry Issues

    Sildenafil 200 mg Troche is recalled for incorrect labeling and being compounded with expired components. Consumers in Texas should check their bottles and contact the manufacturer for instructions.

    Product
    Sildenafil 200 mg Troche (Clinic)
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0820-2020·2020-02-05

    MPRX Recalls Testosterone Topical Cream 4% Due to Expired Components

    MPRX, Inc. dba Medical Park Pharmacy is recalling Testosterone Topical Cream 4% because it was compounded using expired components and has incorrect or missing lot and expiration dates.

    Product
    Testosterone Topical Cream 4%
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0812-2020·2020-02-05

    Progesterone 50 mg Capsules Recalled for Expired Components

    MPRX, Inc. is recalling Progesterone 50 mg capsules compounded with expired components due to incorrect or missing lot and expiration dates.

    Product
    Progesterone 50 mg capsules
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0810-2020·2020-02-05

    Medical Park Pharmacy Recalls Naltrexone Capsules Due to Labeling Errors

    MPRX, Inc. dba Medical Park Pharmacy is recalling Naltrexone 4.5 mg capsules because they were compounded using expired components and have incorrect or missing lot and expiration dates.

    Product
    Naltrexone 4.5 mg capsule
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0823-2020·2020-02-05

    Macleods Pharma Recalls Montelukast Sodium Chewable Tablets for Dissolution Failure

    Macleods Pharma USA is recalling 10,680 bottles of Montelukast Sodium Chewable Tablets, 5 mg, because testing revealed low out-of-specification dissolution results in one lot.

    Product
    MONTELUKAST SODIUM — MONTELUKAST SODIUM (MONTELUKAST SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0824-2020·2020-02-05

    FDA Recalls Nystatin Oral Suspension for Subpotent Assay Levels

    Pharmaceutical Associates Inc. is recalling Nystatin Oral Suspension because it failed potency testing at 12 months. Patients should stop using the product and consult their healthcare provider.

    Product
    NYSTATIN — NYSTATIN (NYSTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0809-2020·2020-02-05

    MPRX Recalls Magic Bullet Supplement Due to Expired Components

    MPRX, Inc. is recalling Magic Bullet Supplement bottles compounded with expired components and incorrect labeling. The recall affects products distributed in Texas.

    Product
    Magic Bullet Supplement
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0821-2020·2020-02-05

    McGuff Compounding Pharmacy Recalls DMPS Injection Due to Particulate Matter

    McGuff Compounding Pharmacy Services, Inc. is recalling Dimercaptopropanesulfonate Sodium (DMPS) injection vials due to the presence of particulate matter.

    Product
    Dimercaptopropanesulfonate Sodium (DMPS), Aqueous injection solution, 50mg/mL 5 mL SDV, Rx only, McGuff Compounding Pharmacy Services, Inc. Santa Ana, CA 92704
    Category
    Drug
    Distribution
    19 states
  • ModerateFDA (Drugs)·D-0808-2020·2020-02-05

    Medical Park Pharmacy Recalls Liothyronine Due to Expired Components

    MPRX, Inc. dba Medical Park Pharmacy is recalling Liothyronine (T3) 92.5 MCG compounded with expired components due to incorrect or missing lot and expiration dates.

    Product
    Liothyronine (T3) 92.5 MCG
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0813-2020·2020-02-05

    Progesterone E4M SR 100 mg capsules recalled for expired components

    MPRX, Inc. is recalling specific lots of compounded Progesterone E4M SR 100 mg capsules because they were made with expired components and have incorrect labeling.

    Product
    Progesterone E4M SR 100 mg capsules
    Category
    Drug
    Distribution
    1 state