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.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

3726–3750 of 17762

HighFDA (Drugs)·D-1156-2022·2022-06-29
Tretinoin Capsules Recalled Nationwide for Failed Dissolution Specifications
Teva Pharmaceuticals is recalling Tretinoin Capsules (10 mg) nationwide due to failed dissolution specifications that may affect medication effectiveness. Patients should contact their pharmacist or doctor to confirm if their prescription is affected.
Product
Tretinoin Capsules, 10 mg, Rx Only, 100 capsules per bottle, Teva Pharmaceuticals USA Inc., North Wales, PA, 19454, NDC 0555-0808-02.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1154-2022·2022-06-29
Testosterone Cypionate Injectable Recalled Due to Manufacturing Sterility Deviation
Sun Pharmaceutical is recalling approximately 47,500 vials of Testosterone Cypionate Injection due to a manufacturing deviation that may have affected product sterility.
Product
TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1151-2022·2022-06-29
Isopropyl Alcohol bottles recalled for defective containers and leakage
Vi-Jon's 70% isopropyl alcohol bottles may leak when squeezed or tilted due to defects in the bottle neck finish. Over 3 million bottles with various lot numbers were distributed nationwide.
Product
ISOPROPYL ALCOHOL — ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1153-2022·2022-06-29
Testosterone Cypionate Injectable Recalled for Manufacturing Quality Issues
Sun Pharmaceutical recalls 97,450 vials of Testosterone Cypionate Injection nationwide due to manufacturing deviations that could cause out-of-specification impurities.
Product
TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1152-2022·2022-06-29
FDA Recalls Clonidine Transdermal Patches for Delivery System Defect
Mayne Pharma is recalling 1,440 cartons of Clonidine transdermal patches nationwide due to an out-of-specification defect in the release liner that could affect proper drug delivery.
Product
CLONIDINE — CLONIDINE (CLONIDINE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1157-2022·2022-06-22
Artri King Tablets Recalled Due to Undeclared Diclofenac
Artri King Reforzado con Ortiga Omega 3 Tablets are being recalled for containing undeclared diclofenac and being marketed without FDA approval. The recall affects 1,308 bottles distributed nationwide.
Product
Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles, Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800, Mexico, D.F., UPC 7 501031 111190.
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-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-1135-2022·2022-06-22
Homeopathic drug Proteus recalled for manufacturing quality control deviations
Washington Homeopathic Products is recalling Proteus homeopathic remedy in multiple potencies due to manufacturing process deviations. The firm initiated this voluntary recall in May 2022.
Product
Proteus, Potency: 7C, 8C, 9C, 12C, 15C, 16C, 20C, 30C, 200C, OTC, Liquid Pellets, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1146-2022·2022-06-22
Medroxyprogesterone acetate injectable suspension recalled for lack of sterility assurance
Sun Pharmaceutical is recalling medroxyprogesterone acetate injectable suspension (150 mg/mL) nationwide due to lack of assurance of sterility. Affected lots contain vials with expiration dates from December 2022 through September 2023.
Product
medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Single-Dose Vial, 150 mg/mL, Rx only, Manufactured for: Northstart Rx LLC, Memphis, TN, 38141, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol Baroda Highway, Halol-389 350, Gujarat India , NDC 16714-981-01
Category
Drug
Distribution
Distributed nationwide
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-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
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-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-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
ModerateFDA (Drugs)·D-1131-2022·2022-06-22
Homeopathic drug Influenzinum recalled for manufacturing process deviations
Washington Homeopathic Products is recalling Influenzinum in multiple potencies due to manufacturing process deviations. The recall affects approximately 6,400 units distributed nationwide.
Product
Influenzinum, Potency: 9X, 10X, 12X, 15X, 25X, 30X, 200C, 12C, 30C 1M, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1138-2022·2022-06-22
Syphilinum homeopathic drug recalled for manufacturing practice deviations
Washington Homeopathic Products is recalling Syphilinum homeopathic products in multiple potencies due to current good manufacturing practice deviations. The affected products were distributed nationwide.
Product
Syphilinum, Potency: 9C, 30C, 200C, 10X, 12X, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1132-2022·2022-06-22
Medorrhinum homeopathic drug recalled for manufacturing process deviations
Washington Homeopathic Products recalled Medorrhinum liquid pellets nationwide due to deviations from manufacturing standards. The product was distributed in 49 glass amber bottles.
Product
Medorrhinum, Potency:12C, 30C, 200C, 1M, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1148-2022·2022-06-22
Premium Nature Hand Sanitizer Recalled for Subpotent Ethanol Content
AMS Packaging is recalling Premium Nature Instant Hand Sanitizer nationwide because FDA analysis found some bottles contain less ethanol than labeled.
Product
Premium Nature Instant Hand Sanitizer, (ethyl alcohol 65%), 8 oz/ 236 ML plastic bottles; Premium Nature, South Plainfield, NJ. UPC 819192028668
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1159-2022·2022-06-22
Artri King Reforzado con Ortiga Omega 3 Tablets Recalled as Unapproved Drug
Walmart Inc is recalling Artri King Reforzado con Ortiga Omega 3 Tablets nationwide because the product was marketed as a drug without FDA approval. All lots are affected.
Product
Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, a) 100-count bottles labeled with UPC 7 501031 111190 and UPC 6 09002 40885, and b) 2 pack of 100-count bottles per carton UPC 3 72426 01434
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1125-2022·2022-06-22
Homeopathic Drug Anthracinum Recalled Over Manufacturing Compliance Deviations
Washington Homeopathic Products is recalling Anthracinum liquid pellets due to manufacturing process deviations. The voluntary recall affects 219 bottles distributed nationwide.
Product
Anthracinum, Potency: 6C, 7C, 8C, 9C, 12C, 14C, 30C, 200C, 11X, 14X, 30X Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1129-2022·2022-06-22
Homeopathic Colibacillinum Drug Recall Due to Manufacturing Deviations
Washington Homeopathic Products recalls Colibacillinum homeopathic drug products due to manufacturing practice deviations. The recall involves 206 bottles distributed nationwide; the manufacturer voluntarily initiated it in May 2022.
Product
Colibacillinum, Potency: 12C, 14C, 15C, 18C, 20C, 30C, Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1140-2022·2022-06-22
Drug recall: Tuberculinum Bovinum due to manufacturing practice deviations
Washington Homeopathic Products is recalling Tuberculinum Bovinum homeopathic remedy due to current good manufacturing practice deviations. No illnesses have been reported.
Product
Tuberculinum Bovinum, Potency: 12C, 30C, 200C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1133-2022·2022-06-22
Homeopathic Drug Morbillinum Recalled for Manufacturing Practice Deviations
Washington Homeopathic Products is recalling Morbillinum in multiple potencies due to manufacturing practice deviations. No illnesses have been reported.
Product
Morbillinum, Potency:7C, 8C, 9C, 10C 12C, 13C, 15C, 20C, 21C, 30C, 200 C,Liquid Pellets, OTC, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
Category
Drug
Distribution
Distributed nationwide

How to read this listing

Filters

3726–3750 of 17762