Phentermine Capsules — Class III drug recall D-1118-2017
Terminated recall by PD-Rx Pharmaceuticals, Inc., reported 2017-08-30, distributed nationwide. Failed Impurities/Degradation Specifications:Out of specification results for individual unknown impurities at
| Recall number | D-1118-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | PD-Rx Pharmaceuticals, Inc., Oklahoma City, OK, United States |
| Recall initiated | 2017-08-11 |
| Classified | 2017-08-23 |
| Reported by FDA | 2017-08-30 |
| Terminated | 2020-01-29 |
| Distributed | Nationwide (US) |
| Quantity | 3,440 bottles |
| Reason classes | specification failure |
| NDC | 55289-0791, 55289-0791-07, 55289-0791-14, 55289-0791-15, 55289-0791-21, 55289-0791-28, 55289-0791-30, 55289-0791-60 |
| Expiration dates | 2017-08-31, 2017-10-31, 2017-12-31 |
Product
Phentermine Capsules, 15 mg, a) 7-count bottle (NDC 55289-791-07), b) 14-count bottle ( NDC 55289-791-14), c) 21-count bottle (NDC 55289-791-21), d) 30-count bottle (NDC 55289-791-30), e) 60-count bottle (NDC 55289-791-60), Packaged by PD-Rx Pharmaceuticals, Incorporated, Oklahoma City, OK. 73127 Mfg: KVK-Tech, Inc. Newtown, PA 18940
Reason for recall
Failed Impurities/Degradation Specifications:Out of specification results for individual unknown impurities at 30th month Room Temperature Retained Sample stabilities test .
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-1118-2017. 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.