Hikma Alendronate Sodium Recall
Hikma Pharmaceuticals is recalling Alendronate Sodium Oral Solution due to out-of-specification assay results in some bottles that were stored on their side. …
Hikma Pharmaceuticals USA INC
Drug & Medication recalls
The newest FDA drug and medication recalls, prescription and over the counter, in plain English. We list the affected lot numbers, the reason for each recall, and whether you should stop taking the product or return it.
178 recalls · updated Sep 17, 2026
B. Braun Dextrose Injection 70% Recall
B. Braun Medical is recalling Dextrose Injection USP 70% in 2000 mL bags due to a lack of sterility assurance and potential leakage from the diaphragm port. …
B BRAUN MEDICAL INC
Wells Pharma Ketamine Injectable Recall
Ketamine Hydrochloride Injectable Solution 50 mg/mL manufactured by Wells Pharma of Houston has been recalled due to manufacturing quality deviations. Stop …
Wells Pharma of Houston LLC
Wells Pharma Fentanyl Citrate Recall
Wells Pharma is recalling fentanyl citrate injectable solution (2500 mcg/250 mL bags) due to manufacturing process deviations that could affect the product's …
Wells Pharma of Houston LLC
Wells Pharma Fentanyl Citrate Injection Recall
Wells Pharma of Houston is recalling fentanyl citrate injectable solution (NDC 73702-203-65) due to manufacturing quality issues that may affect the drug's …
Wells Pharma of Houston LLC
Epinephrine Injection Recall by Amphastar
International Medication Systems is recalling an epinephrine injection due to lack of assurance of sterility. Sterile injectable medications that are not …
International Medication Systems Ltd.
Appco Pharma Prazosin Recall
Appco Pharma has recalled Prazosin Hydrochloride Capsules 2mg due to detection of a potentially harmful impurity (N-nitroso-prazosin) above acceptable limits. …
Appco Pharma LLC
Prazosin Hydrochloride 1mg Capsules Recall
Prazosin Hydrochloride Capsules, USP 1 mg (100-count bottles) manufactured by Appco Pharma LLC for Biocon Pharma Inc. are being recalled because they contain …
Appco Pharma LLC
Taro Fluocinonide Cream 0.05% Recall
Fluocinonide 0.05% Cream (30g tube) is being recalled because the cream's viscosity (thickness) tested above safe limits during quality testing. This may affect …
SUN PHARMACEUTICAL INDUSTRIES INC
Buy-Herbal Kian Pee Wan Capsules Recall
Buy-Herbal's Kian Pee Wan Capsules contain two undeclared prescription drug ingredients, dexamethasone and cyproheptadine, that are not listed on the label and …
Buy-Herbal
Fagron Vancomycin HCI Injection Recall
Fagron's Vancomycin HCI injection is being recalled because it may not be sterile and a plastic piece on the administration port could break off and enter the …
Fagron Compounding Services
MGC Health Cough Drops Recall
MGC Health Sugar Free Honey Lemon Menthol Cough Drops (25-count bags) are being recalled due to quality concerns identified at the manufacturing facility during …
Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
MGC Health Menthol Cough Drops Recall
MGC Health Menthol Cough Drops in Honey Lemon flavor are being recalled due to quality concerns discovered during a manufacturing facility inspection. The FDA …
Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
Exchange Select Cough Drops Recall
Exchange Select Menthol Cough Drops (30-count bags, Honey Lemon flavor) are being recalled due to manufacturing facility quality concerns discovered during an …
Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
Discount Drug Mart Cough Drops Recall
Discount Drug Mart cough drops in 30-count bags are being recalled due to quality concerns identified during an FDA inspection of the manufacturing facility. …
Xiamen Kang Zhongyuan Biotechnology Co., Ltd.
Amneal Tramadol Hydrochloride 50mg Recall
Amneal Pharmaceuticals is recalling Tramadol Hydrochloride 50 mg tablets (500-count bottles) because tests found an impurity called N-nitroso-desmethyl-tramadol …
Amneal Pharmaceuticals, LLC
Clonidine Transdermal System 0.2mg Recall
Clonidine Transdermal System 0.2 mg/day patches supplied by Teva Pharmaceuticals have been recalled because the manufacturer used an unapproved raw material …
Teva Pharmaceuticals USA, Inc
Remedy Gel Hydrocortisone 1% Recall
Remedy Gel hydrocortisone 1% is being recalled because some bottles contain less active ingredient than labeled. If you have this product, stop using it and …
Island Kinetics, Inc. d.b.a. CoValence Laboratories
Amneal Magnesium Sulfate IV Bag Recall 2026
Amneal Pharmaceuticals is recalling specific lots of Magnesium Sulfate IV bags because some pouches labeled as Magnesium Sulfate actually contain Tranexamic …
Amneal Pharmaceuticals, LLC
Teva Octreotide Acetate 20mg Recall
Teva Pharmaceuticals is recalling Octreotide Acetate 20 mg injectable suspension due to sterility concerns from manufacturing defects. The medication may not be …
Teva Pharmaceuticals USA, Inc
Teva Octreotide Acetate 10mg Injection Recall
Teva Pharmaceuticals is recalling Octreotide Acetate 10 mg injectable suspension due to manufacturing quality control failures that mean the sterility of the …
Teva Pharmaceuticals USA, Inc
Cipla Cinacalcet Hydrochloride Recall
Cipla USA is recalling Cinacalcet Hydrochloride 30 mg tablets because they contain higher-than-safe levels of an impurity called N-Nitroso Cinacalcet. Long-term …
Cipla USA, Inc.
Fresenius Kabi Sodium Chloride Injection Recall
Fresenius Kabi is recalling a 0.9% Sodium Chloride Injection due to lack of assurance of sterility. This injectable medication may not be sterile, which could …
Fresenius Kabi USA, LLC
Fresenius Kabi Sodium Chloride Injection Recall
Fresenius Kabi is recalling 0.9% Sodium Chloride Injection due to lack of assurance of sterility. This injectable medication may be contaminated, which could …
Fresenius Kabi USA, LLC
Fresenius Kabi Sodium Chloride Injection Recall
Fresenius Kabi is recalling certain 0.9% Sodium Chloride Injection vials because the manufacturer cannot guarantee they are sterile. Using a non-sterile …
Fresenius Kabi USA, LLC
Fresenius Kabi Sodium Chloride Injection Recall
Fresenius Kabi USA is recalling 0.9% Sodium Chloride Injection 500 mL single-dose bags because the manufacturer cannot confirm the product is sterile. Sterile …
Fresenius Kabi USA, LLC
Fresenius Kabi Sodium Chloride Injection Recall
Fresenius Kabi is recalling 0.45% Sodium Chloride Injection in 250 mL bags because the company cannot guarantee the product is sterile. Non-sterile injectable …
Fresenius Kabi USA, LLC
Payless Compounders Semaglutide Injectable Recall
Semaglutide-Glycine-Cyanocobalamin Injectable vials from Payless Compounders have not been verified as sterile and may be contaminated. Using a non-sterile …
PAYLESS COMPOUNDERS, LLC
Apotex Brimonidine/Timolol Eye Drop Recall
Apotex Corp. is recalling Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution because sterility cannot be assured. Use of a non-sterile eye drop can cause …
Apotex Corp.
Rising Pharma Temozolomide 5mg Recall
Rising Pharmaceuticals is recalling Temozolomide Capsules 5mg due to impurities found during stability testing. The capsules may contain unwanted chemical …
Rising Pharma Holding, Inc.
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