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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10926–10950 of 17785

  • ModerateFDA (Drugs)·D-0500-2017·2017-03-08

    Allegiant Health Recalls HealthA2Z Chewable Aspirin Due to Rubber Particles

    Allegiant Health is recalling HealthA2Z Chewable Aspirin 81 mg because rubber particles were found in the bulk product.

    Product
    HealthA2Z CHEWABLE Aspirin (NSAID) 81 mg, Orange Flavor, 36 Chewable Tablets, a) packaged in 36-count bottle [UPC Code 369168288362 (FP0545)], b) bulk product (6K28817), OTC, Manufactured by: Allegiant Health Deer Park, NY 11729
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0504-2017·2017-03-08

    Perrigo Recalls Salicylic Acid Cream Due to Organic Impurity

    L. Perrigo Company is recalling Salicylic Acid Cream, 6%, due to an out-of-specification organic impurity. The FDA classified this as a Class III recall.

    Product
    Salicylic Acid Cream, 6%, 400g bottle, Rx Only, Manufactured By Perrigo Yeruham, Israel 80500, Distributed By Perrigo Allegan, MI 49010, NDC 45802-806-01, UPC 3 45802-806-01 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0503-2017·2017-03-08

    Perrigo Recalls Salicylic Acid Shampoo Due to Organic Impurity

    L. Perrigo Company is recalling Salicylic Acid Shampoo, 6%, because the active ingredient failed impurity specifications.

    Product
    Salicylic Acid Shampoo, 6%, 177 mL bottle, Rx only, Manufactured By Perrigo Yeruham, Israel, Distributed By Perrigo Allegan, MI 49010, NDC 45802-237-01, UPC 3 45802-237-01 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0509-2017·2017-03-08

    Dr. Reddy's Recalls Zenatane Capsules Due to Dissolution Failure

    Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because they failed to meet dissolution specifications. The recall covers 4,404 cartons distributed nationwide.

    Product
    ZENATANE — ZENATANE (ISOTRETINOIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0475-2017·2017-03-01

    Apotex Recalls Cyclosporine Capsules Due to Impurity Failures

    Apotex Inc. is recalling 19,584 bottles of Cyclosporine Capsules, USP, 100 mg, because the product failed impurity specifications.

    Product
    CYCLOSPORINE — CYCLOSPORINE (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0482-2017·2017-03-01

    RemedyRepack Recalls Glipizide Tablets for Failed Dissolution Specifications

    RemedyRepack Inc. is recalling Glipizide 2.5 mg ER tablets because they failed to meet dissolution specifications. The product was distributed to a customer in Florida.

    Product
    Glipizide 2.5 mg ER Tablets, Manufactured by Watson Laboratories, Inc., Parsippany, NJ 07054, Repackaged by RemedyRepack, Indiana, PA 15701, NDC 52125-0764-02
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0480-2017·2017-03-01

    Hospira Recalls Metronidazole Injection Bags Due to Leaking

    Hospira is recalling 578,784 bags of Metronidazole Injection due to a customer report of a leaking bag, which compromises sterility assurance.

    Product
    METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0483-2017·2017-03-01

    Cherry Hill Sales Recalls Hemorrhoidal Cream Due to Manufacturing Deviations

    Cherry Hill Sales Co. is voluntarily recalling 3,600 cartons of MakeSense Hemorrhoidal Relief Cream due to CGMP deviations.

    Product
    MakeSense PHARMA, HEMORRHOIDAL RELIEF CREAM Phenylephrine HCL-0.25% Zinc Oxide-12.50%,1 oz. (28 g) tube, Made in China, Distributed by Cherry Hill Associates, Chesapeake, VA 23320, NDC 69020-205-28
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0481-2017·2017-03-01

    Sandoz Recalls Transderm Scop Patches Due to Incorrect Labeling Instructions

    Sandoz Inc. is recalling Transderm Scop patches because the outer carton contains incorrect instructions for cutting the patch.

    Product
    Transderm Scop (scopolamine) Transdermal System, 1.5 mg, 1 patch per pouch (NDC 66758-208-58), packaged in 4-count patches per carton (NDC 66758-208-54), Rx Only, Manufactured by ALZA Corporation, Vacaville, CA 95688 for Sandoz Inc., Princeton, NJ 08540.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0485-2017·2017-03-01

    Cherry Hill Sales Recalls Medicated Anti-Itch Cream Due to CGMP Deviations

    Cherry Hill Sales Co. is voluntarily recalling 4,800 cartons of MakeSense PHARMA Medicated Anti-Itch Cream due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    MakeSense PHARMA Medicated ANTI-ITCH CREAM WITH SOOTHING ALOE VERA AND VITAMIN E, Camphor-1% Menthol-1%, 1oz.(28 g) tube, Made in China, Distributed by Cherry Hill Associates, Chesapeake, VA 23320, NDC 69020-201-28
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0487-2017·2017-03-01

    Cherry Hill Sales Recalls Clotrimazole Antifungal Cream Due to CGMP Deviations

    Cherry Hill Sales Co. is voluntarily recalling 2,400 cartons of MakeSense PHARMA ANTIFUNGAL CREAM due to CGMP deviations. The product was distributed in five states.

    Product
    MakeSense PHARMA ANTIFUNGAL CREAM Clotrimazole 1%, 1.25 oz. (35 g) tube, Made in China, Distributed by Cherry Hill Associates, Chesapeake, VA 23320, NDC 69020-203-35
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0486-2017·2017-03-01

    Cherry Hill Sales Recalls MakeSense Antifungal Cream Due to CGMP Deviations

    Cherry Hill Sales Co. is voluntarily recalling 2,400 cartons of MakeSense PHARMA ANTIFUNGAL CREAM due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    MakeSense PHARMA ANTIFUNGAL CREAM 1 oz. Miconazole Nitrate 2%, 1 oz. (28 g) tube, Made in China, Distributed by Cherry Hill Associates, Chesapeake, VA 23320, NDC 69020-208-28
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0484-2017·2017-03-01

    Cherry Hill Sales Recalls MakeSense First Aid Cream Due to CGMP Deviations

    Cherry Hill Sales Co. is voluntarily recalling 7,200 cartons of MakeSense First Aid Cream due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    MakeSense PHARMA FIRST AID CREAM Lidocaine HCL 0.5%, Phenol 0.5%, 1 oz.. (28 g) tube, Made in China, Distributed by Cherry Hill Associates, Chesapeake, VA 23320, NDC 69020-210-28
    Category
    Drug
    Distribution
    5 states
  • CriticalFDA (Drugs)·D-0472-2017·2017-02-22

    MS Bionic Recalls MegaJex Herbal Supplement Containing Unapproved ED Drugs

    MS Bionic is recalling MegaJex Herbal Supplement because it contains sildenafil and tadalafil, active ingredients in approved erectile dysfunction drugs, without FDA approval.

    Product
    MegaJex Herbal Supplement, Maximum Formula for Men, Fast acting, Increase Stamina, 20 capsules, MS Bionics, Gardena, CA
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0474-2017·2017-02-22

    Aurobindo Recalls Venlafaxine Hydrochloride Capsules Due to Physical Defects

    Aurobindo Pharma USA Inc is recalling 47,040 bottles of Venlafaxine Hydrochloride extended-release capsules because some contain punctured or clumped capsules.

    Product
    VENLAFAXINE HYDROCHLORIDE — VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0476-2017·2017-02-22

    Actavis Recalls Glipizide Extended-Release Tablets Due to Dissolution Failure

    Actavis Inc is recalling specific lots of Glipizide extended-release tablets because they failed to meet dissolution specifications at the 10-hour testing point.

    Product
    Glipizide extended-release tablets, 2.5mg, 30-count bottle, Rx Only, Manufactured By Patheon Pharmaceuticals Inc Cincinnati OH 45237 USA, NDC 0591-0900-30, UPC 3-0591090030-4
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0479-2017·2017-02-22

    Teva Recalls Mimvey Lo Tablets Due to Impurity Test Failures

    Teva Pharmaceuticals USA is recalling specific lots of Mimvey Lo tablets because they failed impurity specifications for norethindrone.

    Product
    Mimvey Lo (estradiol and norethindrone acetate tablets USP), 0.5 mg/0.1 mg, 28 tablets per blister card (NDC 0093-5454-18), packaged in 3 blister cards per carton (NDC 0093-5454-62), Rx only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970; Manufactured For: Teva…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0478-2017·2017-02-22

    Accord Healthcare Recalls Lisinopril Tablets Due to Missing Break Line

    Accord Healthcare is recalling 12,896 bottles of 5 mg Lisinopril tablets because the tablets are missing a break line. The recall covers the U.S. and Puerto Rico.

    Product
    Lisinopril tablets, 5 mg, 1000-count bottle, Rx only, Manufactured for Accord Healthcare, Inc., Durham, NC 27703, NDC 16729-376-17
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0477-2017·2017-02-22

    Taclonex Topical Suspension Recalled for Outdated Package Insert

    LEO Pharma Inc. is recalling Taclonex topical suspension because it was packaged with an out-of-date package insert.

    Product
    TACLONEX — TACLONEX (CALCIPOTRIENE AND BETAMETHASONE DIPROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0469-2017·2017-02-15

    VistaPharm Recalls Potassium Chloride Oral Solution Due to Cup Leakage

    VistaPharm is recalling 13,609 cases of Potassium Chloride Oral Solution because the unit dose cups may leak at the seal.

    Product
    Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50 unit dose cups per case (NDC 66689-047-50), Rx only, Xact Dose, Manufactured by VistaPharm, Largo, FL 33771.
    Category
    Drug
    Distribution
    36 states
  • LowFDA (Drugs)·D-0470-2017·2017-02-15

    Aurobindo Recalls Discolored Pantoprazole Sodium Injection Vials

    Aurobindo Pharma USA Inc is recalling 29,800 vials of Pantoprazole Sodium for Injection due to discoloration. The affected vials contain powder with a yellowish-brownish appearance.

    Product
    PANTOPRAZOLE SODIUM — PANTOPRAZOLE SODIUM (PANTOPRAZOLE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0471-2017·2017-02-15

    Apotex Recalls Aripiprazole Tablets Due to Potential Potency Issues

    Apotex Inc. is recalling 67,946 bottles of 2 mg Aripiprazole tablets because the product may not meet specifications throughout its shelf life.

    Product
    Aripiprazole Tablets, 2 mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9; Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-3075-3.
    Category
    Drug
    Distribution
    Distributed nationwide