June 10, 2026DrugsFDA
Guardian Drug Co. Inc. recalls HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 1000 mg, 160-count bottle, Haleon, Warren, NJ 07059, UPC
Hazard: Presence of foreign substance: small metallic particles in chewable tablets.
June 10, 2026DrugsFDA
Guardian Drug Co. Inc. recalls KIRKLAND Signature, ULTRA STRENGTH ANTACID, Calcium Carbonate, 1000 mg, 265-count bottle, MANUFACTURED BY: GUARDIAN DRUG
Hazard: Presence of foreign substance: small metallic particles in chewable tablets.
June 10, 2026DrugsFDA
Ascend Laboratories, LLC recalls Amlodipine and Olmesartan Medoxomil Tablets, 5mg/40mg, Rx Only, 30-count bottle, Manufactured by: Alkem Laboratories Ltd
Hazard: Failed Dissolution Specifications: Olmesartan Medoxomil content below specifications
June 10, 2026DrugsFDA
Asclemed USA Inc. recalls Duloxetine DR Capsules, 30 mg, 30 count bottles, Rx, Relabeled by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC 76
Hazard: CGMP Deviations; presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the FDA acceptable intake limit.
June 10, 2026DrugsFDA
Spectra Medical Devices, Llc recalls Lidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by: Spectra Medical Devices, LLC, Wilmin
Hazard: Lack of Assurance of Sterility
June 10, 2026DrugsFDA
Eugia US LLC recalls Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US
Hazard: Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
June 3, 2026DrugsFDA
AbbVie Inc. recalls PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Sterile, Rx only, Allergen, Inc., an AbbVie co
Hazard: Failed Stability Specifications
June 3, 2026DrugsFDA
AVEVA Drug Delivery Systems, Inc. recalls Nicotine Transdermal System Patch, 14 mg, 14 patches per box, Aveva, Distributed by: RUGBY LABORATORIES, Indianapolis, I
Hazard: Failed Impurities/Degradation Specifications: Elevated levels of oxidative-related impurities, exceeding shelf-life specifications during stability testing of individual units.
May 27, 2026DrugsFDA
Wisconsin Pharmacal Company recalls MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%), NET WT 6 oz (170 g), Manufactured by: Phar
Hazard: Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus.
May 27, 2026DrugsFDA
Safecor Health, LLC recalls Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral Liquid, Contains: Folic Acid 799 mcg/5mL, Delivers 5 m
Hazard: Presence of a Foreign Substance; black particles observed in liquid
May 27, 2026DrugsFDA
IntegraDose Compounding Services LLC recalls fentaNYL Citrate, Sterile CADD for Injection, 2,2500 mcg/50mL in Sterile Water, IntegraDose Compounding Services LLC, 36
Hazard: Subpotent Drug
May 27, 2026DrugsFDA
UCB Biosciences Inc. recalls cimzia (certolizumab pegol), 2x200mg/mL PREFILLED SYRINGES (2 single-dose), Rx ONLY, Manufactured by: UCB Inc., Smyrna,
Hazard: Lack of Assurance of Sterility
May 27, 2026DrugsFDA
Zydus Pharmaceuticals (USA) Inc recalls Erythromycin Tablets, USP, 500 mg, 30 tablets per bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad,
Hazard: CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
May 27, 2026DrugsFDA
Zydus Pharmaceuticals (USA) Inc recalls Erythromycin Tablets, USP, 250 mg, 30 tablets per bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad,
Hazard: CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
May 27, 2026DrugsFDA
ANI Pharmaceuticals, Inc. recalls Estradiol Gel, 0.1%, 0.25 mg, 0.25 g per packet, 30 packets per carton, Rx only, Distributed by: ANI Pharmaceuticals, In
Hazard: Defective Container; packets were found to be either empty or partially full.
May 27, 2026DrugsFDA
Haleon US Holdings LLC recalls Gas-X, Simethicone 125 mg/ ANTIGAS, 120 SoftGels, Distributed by: Haleon, Warren, NJ 07059, UPC: 3 00674 35041 9.
Hazard: Labeling: Not Elsewhere Classified- Incomplete inactive ingredient information on the carton labeling.
May 27, 2026DrugsFDA
Lupin Pharmaceuticals Inc. recalls Liraglutide Injection, 18 mg/3 mL (6 mg/mL), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, M
Hazard: Presence of particulate matter: a white thread-like structure in the cartridge
May 27, 2026DrugsFDA
Sagent Pharmaceuticals recalls Busulfan Injection, 60 mg per 10 mL (6 mg per mL), 8x10 mL Single-Dose Vials, Rx only, Mfd. for Sagent Pharmaceuticals,
Hazard: Failed Impurities/Degradation Specifications
May 27, 2026DrugsFDA
Safecor Health, LLC recalls Atomoxetine Capsules HCL, 10 mg Capsules in unit dose foil strip, strips are packed in cartons of 100, Rx Only, Pkg by:
Hazard: Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.
May 27, 2026DrugsFDA
Amerisource Health Services LLC recalls Primidone Tablets, USP, 50 mg, 100 Tablets (10 x 10 unit dose blister) per carton, Rx only, Distributed by: American Hea
Hazard: Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
May 27, 2026DrugsFDA
Amerisource Health Services LLC recalls Primidone Tablets, USP, 250 mg, 100 Tablets (10 x 10 unit dose blister) per carton, Rx only, Distributed by: American He
Hazard: Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
May 27, 2026DrugsFDA
Golden State Medical Supply Inc. recalls Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, In
Hazard: Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
May 27, 2026DrugsFDA
Golden State Medical Supply Inc. recalls Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Inco
Hazard: Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
May 27, 2026DrugsFDA
Lannett Company Inc. recalls Primidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136,
Hazard: Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
May 20, 2026DrugsFDA
Ascend Laboratories, LLC recalls Ascend Laboratories, LLC, Metoprolol Succinate Extended-Release Tablets, USP, 25 mg* Rx Only, Manufactured by: Alkem Lab
Hazard: Failed Dissolution Specifications
May 20, 2026DrugsFDA
ENDO USA, Inc. recalls Buprenorphine Hydrochloride, Injection, 0.3mg/mL, 5x1 mL Single Dose Vials, Rx only, Manufactured for: Endo USA, Malvern
Hazard: Crystallization; identified as Buprenorphine free base
May 20, 2026DrugsFDA
Oasis Medical, Inc. recalls Oasis Tears PF, Preservative-Free Lubricant Eye Drops, 10mL/0.34 Fl OZ Bottle, Sterile, Manufactured for: OASIS Medical,
Hazard: Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision.
May 13, 2026DrugsFDA
B BRAUN MEDICAL INC recalls Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0
Hazard: Presence of Particulate Matter.
May 13, 2026DrugsFDA
Central Admixture Pharmacy Services, Inc (CAPS) Los Angeles recalls TPN bag (patient specific), Rx# 11-4909703-0-1, Compound Volume 1660 mL per bag, Rx only, Single Dose Injection, Refrige
Hazard: Incorrect Product Formulation: product did not contain insulin as listed in the label.
May 13, 2026DrugsFDA
Acella Pharmaceuticals, LLC recalls NAPROXEN ORAL SUSPENSION, USP, 125 mg/5mL, Rx only, 16fl oz (473 mL) bottles, Distributed by: Acella Pharmaceuticals, LL
Hazard: Chemical contamination; presence of lead and lithium above specification