BD ChloraPrep Hi-Lite Orange Recall
BD ChloraPrep Hi-Lite Orange applicators (a skin antiseptic) were distributed without proper sterilization assurance. These products should have been sterilized …
CareFusion 213, 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.
123 recalls · updated Jun 11, 2026
Methohexital Sodium Injection Recall
Methohexital Sodium for Injection 500 mg multiple dose vials made by OneSource Specialty Pharma have failed quality tests for impurities and degradation. …
ONESOURCE SPECIALTY PHARMA LIMITED
Lacosamide Tablets 100mg Recall
Lacosamide 100mg tablets made by Camber Pharmaceuticals may contain a different medication, Selexipag 1000 mcg, mixed into the bottle. Taking the wrong drug by …
Annora Pharma Private Limited
Gas-X Extra Strength Simethicone 125 mg Recall
Gas-X Extra Strength Simethicone 125 mg softgels have been recalled because a machine leak during packaging may have contaminated the capsules with a diluted …
Haleon US Holdings LLC
Corlanor Ivabradine 7.5mg Recall
Corlanor (ivabradine) 7.5mg tablets in 60-count bottles are being recalled due to the presence of a foreign substance. If you take this medication, stop and …
Amgen, Inc.
Corlanor Ivabradine 5mg Recall
Corlanor (ivabradine) 5 mg tablets are being recalled because bottles may contain a foreign substance. If you take this medication, stop and contact your …
Amgen, Inc.
Rapidol Triple Antibiotic Ointment Recall
Rapidol Triple Antibiotic First Aid Ointment is being recalled because the manufacturer did not follow proper manufacturing standards during production. The FDA …
Dabur India Limited
Med Pride Antibiotic Ointment Recall
Med Pride Triple Antibiotic Ointment packets are recalled due to manufacturing deficiencies that may affect product safety and effectiveness. The maker has …
Dabur India Limited
Med Pride Hydrocortisone Cream Recall
Med Pride Hydrocortisone Cream 1% in 1 oz tubes has been recalled due to manufacturing quality deficiencies found during FDA inspection. The product may not …
Dabur India Limited
Med Pride Bacitracin Zinc Ointment Recall
Med Pride Bacitracin Zinc Ointment is being recalled due to manufacturing quality deficiencies found during an FDA inspection. The ointment may not meet purity …
Dabur India Limited
Lucky Super Soft Antibiotic Ointment Recall
Lucky Super Soft First Aid Triple Antibiotic Ointment is being recalled due to manufacturing quality defects discovered during a FDA inspection. The product may …
Dabur India Limited
Ascend Minocycline 115mg Recall
Ascend Laboratories is recalling Minocycline Hydrochloride Extended-Release Tablets, USP, 115 mg because some bottles failed to meet dissolution specifications …
Ascend Laboratories, LLC
Beekeeper's Naturals Saline Nasal Spray Recall
Beekeeper's Naturals has recalled its 1 fl oz Saline Nasal Spray (Sinus Congestion Rinse, made with Propolis and Xylitol) because the product may be …
BEEKEEPER'S NATURALS USA INC.
Sun Pharmaceutical Budesonide Suspension Recall
Budesonide Inhalation Suspension 1mg/2mL single-dose ampules are being recalled because black or brown specks and particles have been found in the solution. …
SUN PHARMACEUTICAL INDUSTRIES INC
TopCare Health Antacid Tablets Recall
TopCare Health Ultra Strength Antacid Tablets are being recalled because some packages contain small metallic particles in the chewable tablets. These particles …
Guardian Drug Co. Inc.
HyVee Ultra Strength Antacid Recall
HyVee Ultra Strength Antacid tablets may contain small metallic particles. Do not use and return the product for a refund.
Guardian Drug Co. Inc.
HyVee Extra Strength Antacid Recall
HyVee Extra Strength Antacid chewable tablets containing calcium carbonate 750 mg are being recalled due to the presence of small metallic particles in some …
Guardian Drug Co. Inc.
TUMS Calcium Carbonate Antacid Recall
HALEON Calcium Carbonate TUMS Antacid chewable tablets in Assorted Fruit flavor contain small metallic particles that could be a choking or injury hazard. Do …
Guardian Drug Co. Inc.
CAREone Calcium Antacid Recall
CAREone Extra Strength Calcium Antacid tablets may contain small metallic particles. Do not take affected tablets; stop using and contact the seller or …
Guardian Drug Co. Inc.
PureLife Benzocaine Topical Anesthetic Recall
PureLife Topical Anesthetic Gel (Benzocaine 20%, 1 oz, Strawberry Flavor) is being recalled because some bottles may have incomplete seals, which could allow …
Keystone Industries
DHP Topical Anesthetic Gel Recall
DHP Topical Anesthetic Gel (benzocaine 20%, strawberry flavor) is recalled because some bottles may have incomplete seals, which could compromise the product's …
Keystone Industries
IntegraDose Vasopressin Recall
IntegraDose Compounding Services is recalling Vasopressin 2 Units/2 mL syringes because the medication is subpotent, meaning it may not contain the full, …
IntegraDose Compounding Services LLC
Eugia Lidocaine HCl Injection Recall
Eugia is recalling a lidocaine injection because the label wrap covers the barcode, making it difficult to scan. This is a voluntary recall initiated by the …
Eugia US LLC
Spectra Lidocaine HCl Injection Recall
Spectra Medical Devices is recalling Lidocaine HCl Injection because the company cannot guarantee the product is sterile. Non-sterile injectable medications can …
Spectra Medical Devices, Llc
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
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.
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