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Drugs Recalls

17,897 recalls, newest first.

April 29, 2026DrugsFDA
B BRAUN MEDICAL INC recalls Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy Bulk Package, B. Braun Medical Inc., Bethlehem, PA 1801
Hazard: Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.
April 29, 2026DrugsFDA
The Harvard Drug Group LLC recalls Omega-3-Acid, Ethyl Esters, Capsules, USP, 1 gram, 50 capsules (5 x 10 unit dose blister cards) per carton, Rx only, Pac
Hazard: Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells.
April 29, 2026DrugsFDA
Premier Dental Products Co recalls Premier, Monsel's, Ferric Subsulfate Solution, 8 mL bottles, Rx only, Manufacturer: Premier Medical Products, 1710 Roman
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14). It is important to note that this error is limited to the vial itself; the saleable unit of the box of 12 bottles has the correct expiration date printed.
April 29, 2026DrugsFDA
Harrow Eye LLC recalls FRESHKOTE LUBRICANT EYEDROPS, Sterile, 0.33 FL OZ (10mL), Harrow Eye LLC, Nashville, TN USA.
Hazard: Lack of Assurance of Sterility
April 29, 2026DrugsFDA
Leading Pharma, LLC recalls Furosemide Tablets, USP, 80 mg, 100 Tablets bottles, Rx only, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004,
Hazard: CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.
April 29, 2026DrugsFDA
Hetero Labs Limited (Unit V) recalls Pantoprazole Sodium, Delayed-Release Tablets, USP, 40 mg, 1000-count bottle, Rx only, Manufactured for: Camber Pharmaceu
Hazard: Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots."
April 22, 2026DrugsFDA
Huons Co., Ltd. recalls Lidocaine HCl Injection, USP, 2%, 100 mg/5mL (20 mg/mL), 5 mL Single-Dose Vials, Rx only, Manufactured by: Huons Co., Lt
Hazard: Lack of Assurance of Sterility
April 22, 2026DrugsFDA
Huons Co., Ltd. recalls 0.9% Sodium Chloride Injection, USP, 10 mL Ampules, Rx only, Single Dose, Preservative Free, Manufactured for: Spectra M
Hazard: Lack of Assurance of Sterility
April 22, 2026DrugsFDA
Huons Co., Ltd. recalls Bupivacaine Hydrochloride 0.75% in 8.25% Dextrose Injection, USP (15 mg/2 mL) (7.5 mg/mL) ampules, Rx only, Manufactured
Hazard: Lack of Assurance of Sterility
April 22, 2026DrugsFDA
Huons Co., Ltd. recalls Lidocaine HCl injection, USP, 1% 50mg/5mL (10 mg/mL), 5 mL Single Dose Vials, Rx only, Manufactured by: Huons Co, Ltd, C
Hazard: Lack of Assurance of Sterility
April 22, 2026DrugsFDA
Apotex Corp. recalls Desmopressin Nasal Spray, USP, 10 mcg/0.1 mL, 5 mL bottle (50 doses), Rx only, Mfg by: Apotek inc., Toronto, Ontario, Ca
Hazard: Defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners.
April 22, 2026DrugsFDA
Avantor Performance Materials LLC recalls Magnesium Chloride, 6-Hydrate, Crystal, 500G per bottle, Bulk active pharmaceutical ingredient (API), Avantor Performanc
Hazard: Subpotent drug
April 22, 2026DrugsFDA
Island Kinetics, Inc. d.b.a. CoValence Laboratories recalls Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, Skin Script, Chandler, AZ 85226, UPC 6 10563 13873
Hazard: Failed Stability Specifications
April 22, 2026DrugsFDA
The Harvard Drug Group LLC recalls Memantine Hydrochloride Extended-Release, Capsules, 7 mg, 100 Capsules (10 x 10 blister packs), Rx only, Packaged and Di
Hazard: Failed Dissolution Specifications
April 22, 2026DrugsFDA
International Medication Systems Ltd. recalls EPINEPHRINE Injection, USP, 1 mg/10mL (0.1 mg/mL), Rx only, INTERNATIONAL MEDICATION SYSTEMS, LIMITED, So. EL Monte, CA
Hazard: Lack of Assurance of Sterility
April 22, 2026DrugsFDA
Island Kinetics, Inc. d.b.a. CoValence Laboratories recalls Essential Calming Skin Gel, hydrocortisone 1%, 120mL/4oz net wt. (113g) per jar, Distributed By: A.C.E. Inc., DFW Intl.
Hazard: Subpotent Drug
April 22, 2026DrugsFDA
Island Kinetics, Inc. d.b.a. CoValence Laboratories recalls Skin Rehab, Calming Skin Gel, Hydrocortisone Balm, hydrocortisone 1%, .53oz net wt. (15.3g) per bottle, Distributed By:
Hazard: Subpotent Drug
April 22, 2026DrugsFDA
Island Kinetics, Inc. d.b.a. CoValence Laboratories recalls Remedy Gel, hydrocortisone 1%, 30 mL/ 1 fl oz per bottle, Distributed By: glo Skin Beauty, Denver, CO 80216. NDC 66915-
Hazard: Subpotent Drug
April 22, 2026DrugsFDA
Nephron SC, LLC recalls Albuterol Sulfate Inhalation Solution, 0.5%, 25 mg/5 mL (5 mg/mL*), 30x5 mL Sterile Unit-Dose Vials, Rx only, nephron 50
Hazard: Labelling: Illegible label
April 22, 2026DrugsFDA
SUN PHARMACEUTICAL INDUSTRIES INC recalls Fluocinonide, USP, 0.05% Cream, 60g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1,
Hazard: Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
April 22, 2026DrugsFDA
SUN PHARMACEUTICAL INDUSTRIES INC recalls Fluocinonide, USP, 0.05% Cream, 30g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1,
Hazard: Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
April 22, 2026DrugsFDA
SUN PHARMACEUTICAL INDUSTRIES INC recalls Fluocinonide, USP, 0.05% Cream, 15g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1,
Hazard: Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
April 22, 2026DrugsFDA
PAYLESS COMPOUNDERS, LLC recalls Semaglutide-Glycine-Cyanocobalamin Injectable, 2.5 mg, 5 mg, 1 MG/ML, 0.5 mL vials, Rx only, Northwest Compounders, Beav
Hazard: Lack of Assurance of Sterility
April 22, 2026DrugsFDA
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. recalls QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Vanilla Honey Flavor, 30-count bag, Distribut
Hazard: This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
April 22, 2026DrugsFDA
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. recalls QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Menthol Flavor, 30-count bag, Distributed By:
Hazard: This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
April 22, 2026DrugsFDA
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. recalls QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Honey Lemon Flavor, 30-count bag, Distributed
Hazard: This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
April 22, 2026DrugsFDA
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. recalls QC Quality Choice, Pectin Oral Demulcent, Throat Soothing Drops, Creamy Strawberry Flavor, 30-count bag, Distributed By:
Hazard: This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
April 22, 2026DrugsFDA
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. recalls QC Quality Choice, Menthol-Cough Suppressant Oral Anesthetic, Cough Drops, Sugar Free, Honey Lemon Flavor, 25-count bag,
Hazard: This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
April 22, 2026DrugsFDA
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. recalls QC Quality Choice, Menthol- Cough Suppressant Oral Anesthetic, Cough Drops, Cherry Flavor, 30-count bag, Distributed By:
Hazard: This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
April 22, 2026DrugsFDA
Xiamen Kang Zhongyuan Biotechnology Co., Ltd. recalls QC Quality Choice, Menthol- Cough Suppressant Oral Anesthetic, Cough Drops, Sugar Free, Black Cherry Flavor, 25-count ba
Hazard: This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.