CEPHALEXIN MONOHYDRATE CAPSULES — Class II drug recall D-0237-2015
Terminated recall by Physicians Total Care, Inc., reported 2014-11-12, distributed in GA, MO. CGMP deviations: Products were manufactured with active pharmaceutical ingredients that were not manufactured
| Recall number | D-0237-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Physicians Total Care, Inc., Tulsa, OK, United States |
| Recall initiated | 2014-09-22 |
| Classified | 2014-11-05 |
| Reported by FDA | 2014-11-12 |
| Terminated | 2015-03-16 |
| Distributed | GA, MO |
| Reason classes | cgmp |
| Lot numbers | 79MI |
| Expiration dates | 2015-01-31, 2015-06-30 |
Product
CEPHALEXIN MONOHYDRATE CAPSULES,USP, 500 mg, 20-count bottle, Rx only, Manufactured for Caraco Pharmaceuticals, Detroit, MI 48202 by Sun Pharmaceuticals, Fort Worth, TX 76155 and repackaged by Physicians Total Care, Inc., Tulsa, OK 74146-6233
Reason for recall
CGMP deviations: Products were manufactured with active pharmaceutical ingredients that were not manufactured with good manufacturing practices.
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-0237-2015. 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.