Pantoprazole Recall: Camber FD253967 batch 40 mg Rx bottle
The recall involves Pantoprazole Sodium, Delayed-Release Tablets, 40 mg, 1000-count Rx bottles manufactured for Camber Pharmaceuticals and distributed nationwide in the USA. The recall is for Batch FD253967, Exp 06/26/2027, involving 4,740 bottles, due to discoloration described as darker than normal with lighter spots reported in five complaints.
| Brand | Hetero Labs Limited (Unit V) |
|---|---|
| Product | 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 |
| Reason | Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots." |
| Severity | moderate |
| Units affected | 4740 |
| Distribution | Nationwide in the USA. |
| Agency | FDA |
WHAT YOU SHOULD DO
- Do not use tablets from Batch FD253967.
- If you have this batch, contact Camber Pharmaceuticals for return or replacement instructions and follow disposal guidance; keep the bottles in their original packaging unless told otherwise.
- If you have consumed any tablets and feel unwell, contact your healthcare provider for advice.
- Consider reporting adverse events to FDA MedWatch.
How to identify the recalled item
| Lot / date codes | Batch # FD253967, Exp Date: 06/26/2027 |
|---|---|
| Lot / date codes | Batch # FD253967, Exp Date: 06/26/2027 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.