Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
AMPICILLIN CAPSULES Recalled by Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals Due to Labeling: Incorrect Or Missing Package Insert: Product is...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals directly.
Affected Products
AMPICILLIN CAPSULES, USP, 250 mg, 500 count bottles, Rx only, Manufactured for: DAVA Pharmaceuticals, Inc., Fort Lee, NJ, By: Suir Pharma Ireland Ltd., Clonmel, Ireland, NDC: 67253-180-50
Quantity: 360 Bottles
Why Was This Recalled?
Labeling: Incorrect Or Missing Package Insert: Product is labeled with unapproved labeling.
Where Was This Sold?
This product was distributed to 1 state: OH
About Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals has 5 total recalls tracked by RecallDetector.
Related Recalls
Icosapent Ethyl Capsules Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed Tablet/Capsule specifications: Red dots inside capsule and...
Zydus Pharmaceuticals (USA) Inc · March 9, 2026
Product label: Temozolomide Capsules Recalled by Rising Pharma Holding, Inc. Due to Failed Impurities/Degradation Specifications: An out-of-specification result observed during...
Rising Pharma Holding, Inc. · March 3, 2026
Semaglutide Inj. Recalled by New Life Pharma LLC Due to Lack of Assurance of Sterility
New Life Pharma LLC · February 26, 2026
Tirzepatide Inj Recalled by New Life Pharma LLC Due to Lack of Assurance of Sterility
New Life Pharma LLC · February 26, 2026
Tirzepatide Inj Recalled by New Life Pharma LLC Due to Lack of Assurance of Sterility
New Life Pharma LLC · February 26, 2026
Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report