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.

Filters

Agency

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

9651–9675 of 18028

  • CriticalFDA (Drugs)·D-0839-2018·2018-05-23

    Apotex Recalls Subpotent Piperacillin and Tazobactam Injection Vials

    Apotex Inc. is recalling 121,693 vials of Piperacillin and Tazobactam for Injection due to high impurity levels that decreased the drug's potency.

    Product
    Piperacillin and Tazobactam for Injection, USP 3.375 gram/vial* 10-count Single Use Vials per carton, Rx Only, Mfg. by: Hospira Healthcare India Pvt. Ltd. Irungattukottai-602 105, India Mfg. for: Apotex Corp. Weston, FL 33326. NDC 60505-0687-4
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0926-2018·2018-05-23

    AuroMedics Recalls Piperacillin and Tazobactam Injection Due to Glass Particulates

    AuroMedics Pharma LLC is recalling 77,400 vials of Piperacillin and Tazobactam for Injection due to confirmed visible glass particulate matter.

    Product
    PIPERACILLIN AND TAZOBACTAM — PIPERACILLIN AND TAZOBACTAM (PIPERACILLIN SODIUM AND TAZOBACTAM SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0811-2018·2018-05-23

    Milbar Recalls B Prox 10 Anti-blemish Wash Due to Microbial Contamination

    Milbar Laboratories is recalling 3,477 bottles of B Prox 10 Anti-blemish Wash due to microbial contamination. Consumers should stop using the product and return it to the point of purchase.

    Product
    B Prox 10 Anti-blemish Wash, (Benzoyl peroxide 10%), 200 mL bottles, Dermatologic Cosmetic Laboratories, East Haven, CT 06512 USA
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0840-2018·2018-05-23

    Apotex Recalls Subpotent Piperacillin and Tazobactam Injection Vials

    Apotex Inc. is recalling specific lots of Piperacillin and Tazobactam for Injection due to high impurity levels that decreased the drug's potency.

    Product
    Piperacillin and Tazobactam for Injection, USP 4.5 gram/vial* 10-count Single Use Vials per carton, Rx only, Mfg. by: Hospira Healthcare India Pvt. Ltd. Irungattukottai-602 105, India Mfg. for: Apotex Corp. Weston, FL 33326. NDC 60505-0688-4
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0806-2018·2018-05-23

    Prescript Pharmaceuticals Recalls Acetaminophen and Codeine Tablets for Labeling Error

    Prescript Pharmaceuticals is recalling specific lots of Acetaminophen and Codeine Phosphate tablets because the storage temperature instructions on the label differ from the original manufacturer's declaration.

    Product
    ACETAMINOPHEN AND CODEINE PHOSPHATE — ACETAMINOPHEN AND CODEINE PHOSPHATE (ACETAMINOPHEN AND CODEINE PHOSPHATE)
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0820-2018·2018-05-23

    Mylan Recalls Amlodipine and Benazapril Capsules Due to Cleaning Deviations

    Mylan Pharmaceuticals is recalling Amlodipine and Benazapril HCL Capsules because cleaning processes for manufacturing equipment were not followed according to procedure.

    Product
    Amlodipine and Benazapril HCL Capsules, USP, 5 mg/40 mg, 100 count bottles, Mylan Pharmaceuticals, Inc., Morgantown, WV --- NDC 0378-6899-01
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0812-2018·2018-05-23

    Milbar Recalls Solar Defense Sunscreen Due to GMP Deviations

    Milbar Laboratories is recalling 2,156 tubes of Solar Defense Sheer Sunscreen SPF50 due to Good Manufacturing Practice (GMP) deviations.

    Product
    Solar Defense Sheer Sunscreen Broad Spectrum SPF50 (Octinoxate 7.5%, Zinc Oxide 10.5%), 2.5 FL OZ. 74 mL, Distributed by: BeautyRx LLC, NY, NY 10128
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0813-2018·2018-05-23

    Milbar Recalls Naturmetic Sunscreen Due to Manufacturing Deviations

    Milbar Laboratories is recalling 4,815 tubes of Naturmetic SPF 50 Sunscreen due to Good Manufacturing Practice (GMP) deviations.

    Product
    Naturmetic SPF 50 Sunscreen (Octinoxate 7.5%, Zinc Oxide 10.5%), 2.0 fl oz/60mL bottles, Fortis BioPharma, Magnolia, TX 77354.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0819-2018·2018-05-23

    Mylan Recalls Amlodipine and Benazapril Capsules Due to Cleaning Deviations

    Mylan Pharmaceuticals is recalling specific lots of Amlodipine and Benazapril HCL Capsules because the cleaning process for manufacturing equipment was not followed according to procedure.

    Product
    Amlodipine and Benazapril HCL Capsules, USP, 5 mg/10 mg, 100 count bottles, Mylan Pharmaceuticals, Inc., Morgantown, WV --- NDC 0378-6896-01
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0809-2018·2018-05-23

    Prescript Pharmaceuticals Recalls Acetaminophen with Codeine Tablets for Labeling Error

    Prescript Pharmaceuticals is recalling Acetaminophen 300 mg with Codeine Phosphate 30 mg tablets due to a storage temperature labeling discrepancy.

    Product
    Acetaminophen 300 mg with Codeine Phosphate 30 mg tablets, USP, 20-count M-Pak containers, Rx Only. Mnfct for: Mallinckrodt Inc. Hazelwood, MO 63042. Mnfct by:Mallinckrodt Inc. Hazelwood, MO 63042. Pckgd by PreScript Pharm Inc. Pleasanton, CA 94566 NDC: 00406-0484-10 Bar Code 007
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0805-2018·2018-05-23

    Prescript Pharmaceuticals Recalls Clindamycin Capsules Due to Labeling Error

    Prescript Pharmaceuticals is recalling 50 containers of Clindamycin 150 mg capsules in California due to a storage temperature labeling discrepancy.

    Product
    Clindamycin 150 mg capsules, USP, 30-count M-Pak container. Mnfct by: Lannett Co. Inc., Philadelphia, PA. Mnfct for: Lannett Co. Inc., Philadelphia, PA. Pckgd by PreScript Pharm. Inc. Pleasanton, CA 94566. NC 00527-1382-01, Bar Code 0639-30-176
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0808-2018·2018-05-23

    Prescript Pharmaceuticals Recalls Clindamycin Capsules Due to Labeling Error

    Prescript Pharmaceuticals is recalling Clindamycin 300 mg capsules because the storage temperature label differs from the manufacturer's original declaration.

    Product
    Clindamycin 300 mg capsules, USP, 28-count M-Pak containers, Rx Only. Mnfct for: Lannett Co. Inc., Philadelphia, PA 19136. Mnfct. by: Lannett Co. Inc., Philadelphia, PA 19136. Pckgd by PreScript Pharm. Inc., Pleasanton, CA 94566. NDC: 00527-1383-01, Bar Code 0784-28-11
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0814-2018·2018-05-23

    Milbar Recalls MD Complete Clarifying Cleanser Due to GMP Deviations

    Milbar Laboratories is voluntarily recalling 14,491 tubes of MD Complete Clarifying Cleanser due to Good Manufacturing Practice (GMP) deviations.

    Product
    MD Complete Clarifying Cleanser (Salicylic Acid 2.0%), 3 fl oz, (88.7mL), MD Professional LLC, Minneapolis, MN
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0807-2018·2018-05-23

    Prescript Pharmaceuticals Recalls Chlorhexidine Liquid Due to Labeling Error

    Prescript Pharmaceuticals is recalling Chlorhexidine 0.12% liquid due to a storage temperature labeling discrepancy. The product was distributed in California.

    Product
    Chlorhexidine 0.12% liquid, 473 MILLITERS. Rx Only. Mnfct for: XTTRUM Laboratories, Chicago, IL 60609. Mnfct by: pharmaceutical Assoiates, Inc., Greenville, SC 29605. Distrib by: PreScript Pharm. INC., Pleasanton, CA 94588. NDC: 00116-2001-16, Bar Code 1385-38-482
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0815-2018·2018-05-23

    Pharmalucence Recalls Technetium TC 99M Mebrofenin Kits for Stability Failures

    Pharmalucence, Inc. is recalling Technetium TC 99M Mebrofenin kits nationwide because they failed stability specifications.

    Product
    KIT FOR THE PREPARATION OF TECHNETIUM TC 99M MEBROFENIN — KIT FOR THE PREPARATION OF TECHNETIUM TC 99M MEBROFENIN (KIT FOR THE PREPARATION OF TECHNETIUM TC 99M MEBROFENIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0802-2018·2018-05-23

    Sun Pharma Recalls Sulfamethoxazole and Trimethoprim Tablets Due to Foreign Matter

    Sun Pharmaceutical Industries is recalling one lot of Sulfamethoxazole and Trimethoprim tablets because polyethylene was detected in two tablets.

    Product
    SULFAMETHOXAZOLE AND TRIMETHOPRIM — SULFAMETHOXAZOLE AND TRIMETHOPRIM (SULFAMETHOXAZOLE AND TRIMETHOPRIM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0803-2018·2018-05-23

    Boiron Recalls Calendula Cream Due to Outer Carton Labeling Error

    Boiron Inc. is recalling 52,810 tubes of Calendula Cream because the outer carton incorrectly lists the active ingredient concentration as 7% instead of 10%.

    Product
    Calendula Cream, calendula officinalis 1X HUS-10%, 2.5 oz. tubes, Distributed by Boiron Inc., Newtown Square, PA
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0810-2018·2018-05-23

    Aidarex Recalls Ferrous Sulfate Tablets Due to Foreign Material Presence

    Aidarex Pharmaceuticals LLC is recalling 450 bottles of Ferrous Sulfate 325 MG tablets distributed in Florida because foreign tablets or capsules were found in the product.

    Product
    Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00
    Category
    Drug
    Distribution
    1 state
  • LowFDA (Drugs)·D-0818-2018·2018-05-23

    Sun Pharma Recalls Riomet Metformin Solution Due to Labeling Errors

    Sun Pharmaceutical Industries is recalling Riomet (metformin hydrochloride) oral solution due to identified labeling discrepancies in the patient literature.

    Product
    RIOMET — RIOMET (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0791-2018·2018-05-16

    Kroger Specialty Pharmacy Recalls Capecitabine Tablets Due to Processing Controls

    Kroger Specialty Pharmacy is recalling Capecitabine 500 mg tablets due to a lack of processing controls. The affected lots were dispensed in five states between December 2017 and February 2018.

    Product
    Capecitabine 500 mg Tablet NDC 00378-2512-78 28 days supply and 21 days supply
    Category
    Drug
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0730-2018·2018-05-16

    Vitalab Pharmacy Recalls Sterile Injectable Drug Due to Sterility Concerns

    Vitalab Pharmacy is recalling 22 vials of a sterile injectable drug because airflow patterns may not support aseptic production, raising sterility concerns.

    Product
    Papaverine 9mg/Phentolamine 1mg/Atropine 0.1mg/Prostaglandinl 10mcg/ml, sterile injectable, Vitalab Pharmacy, Inc
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Food)·F-1401-2018·2018-05-16

    FDA Recalls Energique Herbal Supplements for Unapproved Drug Claims

    Grato Holdings is recalling Energique herbal supplements because they are marketed as unapproved new drugs based on disease claims.

    Product
    Energique, Herbal Supplement, Octocom,; Dist. by Energique, Inc. Woodbine, IA 51579
    Category
    Drug
    Distribution
    Distributed nationwide