CVS pharmacy Original Strength Acid Controller tablets — Class III drug recall D-1058-2016
Terminated recall by Dr. Reddy's Laboratories, Inc., reported 2016-07-06, distributed nationwide. Failed impurities/degradation specification: An out of specification results has been determined for an indivi
| Recall number | D-1058-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Dr. Reddy's Laboratories, Inc., Princeton, NJ, United States |
| Recall initiated | 2016-04-22 |
| Classified | 2016-06-30 |
| Reported by FDA | 2016-07-06 |
| Terminated | 2017-04-26 |
| Distributed | Nationwide (US) |
| Quantity | 84,240 bottles |
| Reason classes | specification failure |
| Lot numbers | 79405008A, 79405008B, 79405008C |
| Expiration dates | 2017-05 |
Product
CVS pharmacy Original Strength Acid Controller tablets, 10 mg, 30-count bottle, OTC, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, UPC 150049523
Reason for recall
Failed impurities/degradation specification: An out of specification results has been determined for an individual related substance during stability testing at the 18th month interval for the Famotidine 10 mg Tablet, USP.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1058-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.