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.
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.
133 recalls · updated Jul 16, 2026
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.
Farmhouse Fresh Midnight Clearing Lotion Recall
FarmHouse Fresh Midnight Clearing Night Lotion (2.5% benzoyl peroxide acne treatment) has been recalled due to benzene contamination. Benzene is a known …
Owen Biosciences Inc.
Artificial Tears Eye Drops Recall
Artificial Tears Sterile Lubricant Eye Drops sold under multiple store brands are being recalled because the manufacturer cannot guarantee they remain sterile. …
K.C. Pharmaceuticals, Inc
Somgem Pig & Yomin Toilet Lighter Recall
Somgem Lightweight Tiny Pinky Pig and Yomin Toilet novelty lighters have been recalled because they lack the required child-resistant mechanisms. Without this …
Somgem Lightweight Tiny Pinky Pig and Yomin Toilet Lighters
Nomida Semaglutide Recall
Nomida semaglutide 2 mg injectable vials are being recalled due to lack of assurance of sterility. Non-sterile injections can cause serious infections.
New Life Pharma LLC
Macleods Levothyroxine Sodium 150mcg Recall
Levothyroxine Sodium 150 mcg tablets manufactured for Macleods Pharma USA are being recalled because they contain lower active ingredient than labeled, which …
MACLEODS PHARMA USA, INC
Cipla Nilotinib 150 mg Capsules Recall
Cipla USA is recalling Nilotinib 150 mg capsules due to failed stability tests showing changes in appearance and description during long-term storage. The …
Cipla USA, Inc.
MAXIMUM ZONE 2 Lidocaine Cream Recall
MAXIMUM ZONE 2 4% Lidocaine Cream (containing lidocaine and epinephrine) is being recalled because stability testing does not support the listed expiry date. …
HTO Nevada Inc. dba Kirkman
Five-Star Vasocaine Spray Recall
Five-Star Vasocaine Spray (lidocaine and racepinephrine) in 4 oz bottles has been recalled because the drug's stability is uncertain and may not remain safe …
HTO Nevada Inc. dba Kirkman
Midodrine Hydrochloride 5 mg Recall
Midodrine Hydrochloride Tablets 5 mg (50 tablets in blister packs) have been recalled due to inadequately sealed blister packaging. The defective container can …
The Harvard Drug Group LLC
Harbin Jixianglong Semaglutide Recall
Harbin Jixianglong Biotech is recalling semaglutide powder used for pharmacy compounding due to incomplete process and bacterial endotoxin testing before …
Harbin Jixianglong Biotech Co., Ltd.
Eptifibatide Injection Recall - Labeling Error
Eptifibatide Injection 75 mg/100 mL vials distributed by Slate Run Pharmaceuticals have incorrect labeling on the carton. The label says "for weight-adjusted …
Slate Run Pharmaceuticals
Fresenius Kabi Vancomycin Recall
Fresenius Kabi Compounding is recalling vancomycin HCl in 0.9% Sodium Chloride Injection because the manufacturer cannot ensure the product is sterile. Patients …
Fresenius Kabi Compounding, LLC
Fresenius Kabi Thiamine HCl Injection Recall
Fresenius Kabi's thiamine HCl injection cannot be guaranteed to be sterile, which could allow bacteria or other contaminants into the bloodstream. Healthcare …
Fresenius Kabi Compounding, LLC
Fresenius Kabi Ketamine HCl Recall
Fresenius Kabi is recalling ketamine HCl injections due to lack of assurance of sterility. Non-sterile injectable drugs can cause serious infections.
Fresenius Kabi Compounding, LLC
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