Drug Recall Records

This page shows recent human drug recall alerts sourced from the FDA. It includes current and some previously imported records, but is not a complete historical archive of all past recalls. For full historical data, visit the official FDA Drug Recalls page. Always consult a healthcare professional for medical advice.

Search
By Dosage Form:
AllTabletsCapsulesInjectables
By Recall Category:
AllContamination / SterilityLabeling / PackagingUndeclared Ingredient
Fresenius Kabi – Morphine Sulfate Injection USP, Simplist® 2 mg/1 mL
Date: 08/05/2026
Brand: Fresenius Kabi
Product: Morphine Sulfate Injection USP, Simplist® 2 mg/1 mL
Company: Fresenius Kabi
Recall Reason: Due to a label mix-up
Dosage Form: Injection
Category: Labeling / Packaging
View Details View FDA Recall Listings
VMC – Compounded Glutathione 200 mg/mL Multi-Dose Vials
Date: 08/05/2026
Brand: VMC
Product: Compounded Glutathione 200 mg/mL Multi-Dose Vials
Company: Victory Medical Center Pharmacy
Recall Reason: Elevated Endotoxin level
Dosage Form: Other / Unspecified
Category: Quality / Potency
View Details View FDA Recall Listings
OPTIRAY – OPTIRAY Imaging Bulk Package (IBP) 350, 500mL in vial (Ioversol Injection 74% 350 mg iodine/ml)
Date: 08/04/2026
Brand: OPTIRAY
Product: OPTIRAY Imaging Bulk Package (IBP) 350, 500mL in vial (Ioversol Injection 74% 350 mg iodine/ml)
Company: Liebel-Flarsheim Company, LLC
Recall Reason: Presence of particulate matter comprising polyethylene and other plastic materials, stainless steel and glass
Dosage Form: Injection
Category: Other Recall Issue
View Details View FDA Recall Listings
American Regent, Inc. – Papaverine Hydrochloride Injection, USP 60 mg/ 2 mL
Date: 07/27/2026
Brand: American Regent, Inc.
Product: Papaverine Hydrochloride Injection, USP 60 mg/ 2 mL
Company: American Regent, Inc.
Recall Reason: Products were found to contain particulate matter
Dosage Form: Injection
Category: Other Recall Issue
View Details View FDA Recall Listings
Long Grove Pharmaceuticals – Cyclophosphamide for Injection
Date: 07/24/2026
Brand: Long Grove Pharmaceuticals
Product: Cyclophosphamide for Injection
Company: Sunny Pharmtech, Inc.
Recall Reason: Presence of particulate matter identified as steel
Dosage Form: Injection
Category: Other Recall Issue
View Details View FDA Recall Listings
Baxter – Cefazolin in Dextrose Injection
Date: 07/24/2026
Brand: Baxter
Product: Cefazolin in Dextrose Injection
Company: Baxter International Inc.
Recall Reason: Particulate matter (cardboard) found in the solution.
Dosage Form: Injection
Category: Other Recall Issue
View Details View FDA Recall Listings
Rising Pharma Holdings Inc. – Cetirizine Hydrochloride Tablets USP 5 mg
Date: 07/20/2026
Brand: Rising Pharma Holdings Inc.
Product: Cetirizine Hydrochloride Tablets USP 5 mg
Company: Unique Pharmaceutical Laboratories
Recall Reason: Potential cross contamination with Ranitidine
Dosage Form: Tablet
Category: Contamination / Sterility
View Details View FDA Recall Listings
Gas-X – Gass-X Extra Strength Softgels 120 and 72ct
Date: 06/04/2026
Brand: Gas-X
Product: Gass-X Extra Strength Softgels 120 and 72ct
Company: Haleon
Recall Reason: Potential chemical contamination
Dosage Form: Other / Unspecified
Category: Contamination / Sterility
View Details View FDA Recall Listings
Best Supplements Best Prices – Dietary supplement for sexual enhancement
Date: 05/18/2026
Brand: Best Supplements Best Prices
Product: Dietary supplement for sexual enhancement
Company: Best Supplements Best Prices
Recall Reason: Undeclared Sildenafil, Tadalafil, and Flibanserin
Dosage Form: Other / Unspecified
Category: Undeclared / Unapproved Ingredient
View Details View FDA Recall Listings
Aisling – DOXOrubicin Hydrochloride Liposome Injection 50mg/25 mL
Date: 05/13/2026
Brand: Aisling
Product: DOXOrubicin Hydrochloride Liposome Injection 50mg/25 mL
Company: Sun Pharmaceutical Industries, Inc.
Recall Reason: Presence of glass particles
Dosage Form: Injection
Category: Other Recall Issue
View Details View FDA Recall Listings
B. Braun – Lactated Ringer’s Injection, E7500, 1L
Date: 04/28/2026
Brand: B. Braun
Product: Lactated Ringer’s Injection, E7500, 1L
Company: B. Braun Medical Inc.
Recall Reason: Products were found to contain particulate matter in solution
Dosage Form: Injection
Category: Other Recall Issue
View Details View FDA Recall Listings
Kian Pee Wan – Dietary supplement capsules marketed for treatment for gaining weight and stimulating appetite.
Date: 04/01/2026
Brand: Kian Pee Wan
Product: Dietary supplement capsules marketed for treatment for gaining weight and stimulating appetite.
Company: Aphreseller
Recall Reason: Device & Drug Safety/Unapproved Drug
Dosage Form: Capsule
Category: Other Recall Issue
View Details View FDA Recall Listings
1
2
3
…
10
Next »