United StatesPantoprazole Sodium delayed‑release tablets USP 40 mg in 1,000‑count bottles (NDC 31722-713-10), batch # FD253967, exp. 06/26/2027, manufactured by Hetero Labs Limited for Camber Pharmaceuticals, are being recalled. The recall follows five complaints that tablets were discolored darker than normal and had lighter‑colored spots.
What's being recalled
Pantoprazole Sodium, Delayed-Release Tablets, USP, 40 mg, 1000-count bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, By: Hetero, Hetero Labs Limited, Unit V, Polepally, Jadcherta, Mahabubager-509 301, India, NDC 31722-713-10
Recalling firm: Hetero Labs Limited (Unit V), Mahabubnagar, N/A, India.
How to identify it
Batch # FD253967, Exp Date: 06/26/2027
The hazard
Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots."
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Nationwide in the USA.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)