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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5676–5700 of 17772

  • SevereFDA (Drugs)·D-0081-2021·2020-11-25

    Hand Sanitizer Recalled for Methanol Contamination and Low Ethanol Content

    Albek De Mexico is recalling Assured Instant Hand Sanitizer bottles because they contained methanol and had lower ethanol levels than labeled.

    Product
    Assured Instant Hand Sanitizer Vitamin E and Aloe (Ethyl Alcohol 70% v/v), 8 fl oz/ 237 mL bottle, Distributed By: Greenbrier International, Inc. 500 Volvo Parkway, Chesapeake, VA 23320. Made in Mexico, UPC 639277928597
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0097-2021·2020-11-25

    Ascent Pharmaceuticals Recalls Hydrocodone and Acetaminophen Tablets Due to Foreign Tablet

    Ascent Pharmaceuticals is recalling 9,768 bottles of Hydrocodone Bitartrate and Acetaminophen Tablets because one bottle contained a Losartan Potassium tablet.

    Product
    Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325mg 100-count bottles, Rx Only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc. Central Islip, NY 11722, NDC 31722-943-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0082-2021·2020-11-25

    Next Advanced Antibacterial Hand Sanitizer Recalled for Methanol Contamination

    Albek De Mexico S.A. De C.V. is recalling Next Advanced Antibacterial Hand Sanitizer because it contained methanol and had lower ethanol levels than labeled.

    Product
    NEXT ADVANCED ANTIBACTERIAL HAND SANITIZER (Ethyl Alcohol 70%), 8 FL OZ (236 ML) bottle, Made in Mexico, Distributed by: Genomma Lab USA Inc., Houston, TX 77027. UPC 6 50240 05357 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0079-2021·2020-11-25

    Hand Sanitizer Recalled for Methanol Contamination and Low Ethanol Content

    Albek De Mexico S.A. De C.V. is recalling Modesa Instant Hand Sanitizer because it contained methanol and had lower ethanol content than labeled.

    Product
    Modesa INSTANT HAND SANITIZER with Moisturizers and Aloe Vera (ethyl alcohol 70% v/v) 8 fl oz (237 mL) bottle, Distributed by: Midwood brands, LLC 10611 Monroe RD. Mathews, NC 28105 Made in Mexico UPC 3 2251 38042 6
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0077-2021·2020-11-25

    Preferred Pharmaceuticals Recalls Metformin HCl Extended Release Tablets Due to NDMA

    Preferred Pharmaceuticals is recalling 99 bottles of Metformin HCl Extended Release Tablets because FDA analysis detected N-Nitrosodimethylamine (NDMA) levels exceeding the Acceptable Daily Intake Limit.

    Product
    Metformin HCl Extended Release Tablets USP 500 mg, Generic for : Glucophage XR, Pkg Size 100, Mfg: Time-Cap Labs, Inc.; Farmingdale, NY, NDC #: 68788-6932-1, Preferred Pharmaceuticals, Inc.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0080-2021·2020-11-25

    Assured Instant Hand Sanitizer Recalled for Methanol Contamination

    Albek De Mexico S.A. De C.V. is recalling 27,000 bottles of Assured Instant Hand Sanitizer because the product contained methanol and was below the label claim for ethanol content.

    Product
    Assured Instant Hand Sanitizer Aloe & Moisturizers (Ethyl Alcohol 70% v/v) 8 fl oz / 237 mL bottle, Distributed By: Greenbrier International, Inc. 500 Volvo Parkway, Chesapeake, VA 23320. Made in Mexico.UPC 639277928610
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0078-2021·2020-11-25

    Hand Sanitizer Recalled for Methanol Contamination and Low Ethanol Content

    Albek De Mexico S.A. De C.V. is recalling NuuxSan hand sanitizer because it contained methanol and had lower ethanol levels than labeled.

    Product
    NuuxSan Instant ANTIBACTERIAL HAND SANITIZER, 70% Ethyl Alcohol (ethyl alcohol 70%), 8 fl oz. 237 mL bottle, Distributed by PCM North America LLC 9543 Bassonnet ST. STE 307, Houston, TX 77036, Made in Mexico, UPC 7 13620 00017 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0084-2021·2020-11-25

    Milbar Recalls DCL B Prox10 Anti-Blemish Wash Due to GMP Deviations

    Milbar Laboratories is voluntarily recalling 7,591 bottles of DCL B Prox10 Anti-Blemish Wash due to Good Manufacturing Practice (GMP) deviations.

    Product
    DCL B Prox10 Anti-Blemish Wash (Benzoyl Peroxide 10%), 200 ml/6.7 fl.oz. Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA, UPC 0357486500853
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0087-2021·2020-11-25

    Milbar Recalls DCL T Shampoo for GMP Deviations

    Milbar Laboratories is voluntarily recalling 1,225 bottles of DCL T Shampoo due to Good Manufacturing Practice (GMP) deviations.

    Product
    DCL T Shampoo for Hair and Body ( Solution Coal Tar U.S.P. 3% and 0.6% Coal Tar), 300 ml/ 10.1 fl.oz. Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA, UPC 3574865069947
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0099-2021·2020-11-25

    Grato Holdings Recalls Homeopathic Energy Catalyst for Undeclared API

    Grato Holdings is recalling 399 bottles of Homeopathic Energy Catalyst due to an undeclared active pharmaceutical ingredient and incorrect formulation.

    Product
    Homeopathic Energy Catalyst, 1 fl oz (30 mL) Distributed by: Deseret Biologicals, Inc. 469 W. Parkland Drive Sandy, UT 84070. NDC 43742-0756-1.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0094-2021·2020-11-25

    Milbar Recalls DCL Alpha Beta Gel Toner Due to GMP Deviations

    Milbar Laboratories is voluntarily recalling DCL Alpha Beta Gel Toner due to Good Manufacturing Practice (GMP) deviations. The product was distributed nationwide and internationally.

    Product
    DCL Alpha Beta Gel Toner (1.95% Salicylic Acid) 200 mL/6.7 fl. oz, Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0083-2021·2020-11-25

    Milbar Recalls DCL Active Mattifying Cleanser Due to GMP Deviations

    Milbar Laboratories is recalling 4,878 tubes of DCL Active Mattifying Cleanser due to Good Manufacturing Practice (GMP) deviations. The product was distributed nationwide and internationally.

    Product
    DCL Active Mattifying Cleanser (Salicylic Acid 2%), 125mL/4.2 fl.oz. Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA, UPC 357486509627
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0092-2021·2020-11-25

    Milbar Recalls Willa Clear Skin Salicylic Acid Tubes Due to GMP Deviations

    Milbar Laboratories is voluntarily recalling 4,855 tubes of Willa Clear Skin (Salicylic Acid 2%) due to Good Manufacturing Practice (GMP) deviations. The product was distributed nationwide and internationally.

    Product
    Willa Clear Skin (Salicylic Acid 2%), 4.2 fl oz 124ml tubes, WBC Group LLC, Dist. Chandler, AZ 85226
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0089-2021·2020-11-25

    Milbar Recalls Malin + Goetz Salicylic Gel Due to GMP Deviations

    Milbar Laboratories is recalling 2,664 tubes of Malin + Goetz Salicylic Gel due to Good Manufacturing Practice (GMP) deviations.

    Product
    (Malin + Goetz) Salicylic Gel (2% Salicylic Acid) 0.5 fl.oz. 15 mL tube, Distributed by: Malin+Goetz Inc 330 Seventh Avenue, New York, New York, 10001
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0096-2021·2020-11-25

    Milbar Recalls Salicylic Acid Shampoo Due to GMP Deviations

    Milbar Laboratories is recalling Salicylic Acid Shampoo 3% due to Good Manufacturing Practice deviations. The product was distributed in the US and internationally.

    Product
    Salicylic Acid Shampoo 3%, Bulk Product, 360 Therapeutics
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0086-2021·2020-11-25

    Milbar Recalls DCL SA Scalp Therapy Shampoo Due to GMP Deviations

    Milbar Laboratories is recalling 1,815 bottles of DCL SA Scalp Therapy Shampoo due to Good Manufacturing Practice (GMP) deviations.

    Product
    DCL SA Scalp Therapy Shampoo (Salicylic Acid 3%) 300 ml/10.1 fl.oz. Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA, UPC 357486503120
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0093-2021·2020-11-25

    Milbar Recalls Willa Pore Perfector Pads Due to GMP Deviations

    Milbar Laboratories is recalling 2,638 jars of Willa Pore Perfector pads due to Good Manufacturing Practice deviations. The product was distributed nationwide and internationally.

    Product
    Willa Pore Perfector (Salicylic Acid 2%) pads, 30 pads
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0088-2021·2020-11-25

    Milbar Recalls Malin + Goetz Dandruff Shampoo Due to GMP Deviations

    Milbar Laboratories is recalling 5,312 bottles of Malin + Goetz dandruff shampoo due to Good Manufacturing Practice deviations.

    Product
    (Malin + Goetz) dandruff Shampoo Psoriasis and Sebborrheic Dermatitis (1.9% Pyrithione Zinc) 8 fl.oz bottle, Distributed by: Malin+Goetz Inc 330 Seventh Avenue, New York, New York, 10001
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0090-2021·2020-11-25

    Milbar Recalls Malin+Goetz SPF 30 Face Moisturizer Due to GMP Deviations

    Milbar Laboratories is recalling 3,692 tubes of Malin+Goetz SPF 30 Face Moisturizer due to Good Manufacturing Practice (GMP) deviations.

    Product
    (Malin+Goetz) spf 30 face moisturizer (Avobenzone 3%, Homosalate 10 %, Octinoxate 7.5%, Octisalate 2.75%, Oxybenzone 5%) 1.7 fl. oz. 50 ml tubes, Distributed by: Malin+Goetz Inc 330 Seventh Avenue, New York, New York, 10001
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0106-2021·2020-11-25

    Apotex Recalls Aripiprazole Tablets Due to Dissolution Failures

    Apotex Corp. is recalling Aripiprazole Tablets 15 mg because they failed to meet dissolution specifications. The affected products were distributed nationwide in the USA.

    Product
    Aripiprazole Tablets, USP 15 mg tablets, packaged in a) 1000 count bottle, NDC 60505-2675-8; b) 30 count bottle, NDC 60505-2675-3; Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0101-2021·2020-11-25

    Hikma Recalls Sodium Chloride Injection Vials Due to pH Failures

    Hikma Pharmaceuticals is recalling specific lots of Sodium Chloride Injection USP 0.9% 2 mL vials because they failed pH specifications.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0085-2021·2020-11-25

    Milbar Recalls DCL AHA Lightening Gel Due to GMP Deviations

    Milbar Laboratories is recalling 1,608 bottles of DCL AHA Lightening Gel due to Good Manufacturing Practice deviations. The product was distributed nationwide and internationally.

    Product
    DCL AHA Lightening Gel (hydroquinone 2%), 30 ml/1 fl.oz. Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA, UPC 357486500471
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0091-2021·2020-11-25

    Milbar Recalls MD Complete Breakout Treatment Due to GMP Deviations

    Milbar Laboratories is voluntarily recalling 2,655 bottles of MD Complete Breakout Treatment due to Good Manufacturing Practice deviations.

    Product
    MD Complete Breakout Treatment (Benzoyl Peroxide 4.5%) 1 fl. oz. (30mL) bottles, MD Professional LLC, Minneapolis, MN
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0095-2021·2020-11-25

    Milbar Recalls DCL Clear Skin Anti-Blemish Hydrator Due to GMP Deviations

    Milbar Laboratories is voluntarily recalling 927 tubes of DCL Clear Skin Anti-Blemish Hydrator due to Good Manufacturing Practice (GMP) deviations.

    Product
    DCL Clear Skin Anti-Blemish Hydrator (2% Salicylic Acid), 50ml/1.7 fl. oz, Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA
    Category
    Drug
    Distribution
    1 state