IntegraDose Fentanyl Citrate Injection Recall
IntegraDose Compounding Services is recalling fentanyl citrate sterile injection (2,500 mcg/50mL) because the doses are subpotent, meaning they contain less …
IntegraDose Compounding Services LLC
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.
97 recalls · updated May 12, 2026
Safecor Atomoxetine 10mg Recall
Safecor Health is recalling Atomoxetine Capsules labeled as 10 mg because some capsules actually contain 25 mg due to a labeling error. Taking the wrong dose of …
Safecor Health, LLC
Zydus Erythromycin 500 mg Tablets Recall
Zydus Pharmaceuticals is recalling Erythromycin 500 mg tablets because they contain higher-than-safe levels of a potentially harmful chemical. If you take this …
Zydus Pharmaceuticals (USA) Inc
Oasis Tears PF Eye Drops Recall
Oasis Tears PF preservative-free lubricant eye drops are being recalled due to lack of assurance of sterility. Non-sterile eye drops can cause serious eye …
Oasis Medical, Inc.
Lupin Liraglutide Injection Recall
Lupin Pharmaceuticals has recalled Liraglutide Injection 18 mg/3 mL due to the presence of a white thread-like structure found in some cartridges. Using a …
Lupin Pharmaceuticals Inc.
Similasan iVIZIA Eye Drops Recall
Similasan iVIZIA Sterile Lubricant Eye Drops (0.33 fl oz) are being recalled because the manufacturer did not maintain proper sterility safeguards during …
Thea Pharma, Inc.
IVIZIA Lubricant Eye Drops Recall
IVIZIA Sterile Lubricant Eye Drops have been recalled because the FDA found manufacturing safety issues that affect sterility. If you use this product, stop use …
Thea Pharma, Inc.
GenTeal Tears Eye Gel Recall
GenTeal Tears Lubricant Eye Gel is being recalled because the manufacturer cannot assure the product is sterile. Use of a non-sterile eye product can cause …
Alcon Research LLC
FreshKote Lubricant EyeDrops Recall
FreshKote Lubricant EyeDrops are being recalled because the manufacturer cannot guarantee the product's sterility. Non-sterile eyedrops can cause serious eye …
Harrow Eye LLC
Omega-3-Acid Ethyl Esters Capsules Recall
The Harvard Drug Group is recalling Omega-3-Acid Ethyl Esters capsules because the capsule shells failed stability testing and do not meet specifications for …
The Harvard Drug Group LLC
Apotex Desmopressin Nasal Spray Recall
Apotex is recalling Desmopressin Nasal Spray due to defective bottle caps with dislodged or missing cap liners, which could compromise the integrity of the …
Apotex Corp.
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
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
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
Get free recall alerts
New Drug & Medication recalls, the moment they post.
Free forever. Unsubscribe anytime. We never sell your data.