Phentermine — Class III drug recall D-1162-2017
Terminated recall by Aidarex Pharmaceuticals LLC, reported 2017-09-20, distributed in CA, NV. Failed Impurities/Degradation Specification; out-of-specification results for individual unknown impurities at
| Recall number | D-1162-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aidarex Pharmaceuticals LLC, Corona, CA, United States |
| Recall initiated | 2017-09-05 |
| Classified | 2017-09-13 |
| Reported by FDA | 2017-09-20 |
| Terminated | 2019-12-04 |
| Distributed | CA, NV |
| Quantity | 35 bottles |
| Reason classes | specification failure |
| NDC | 33261-0361-30 |
| Lot numbers | 47262-2, 47262-3, 47262-4, 47262-5, 47262-6, 47262-7 |
| Expiration dates | 2017-08-31, 2017-12-30, 2017-12-31 |
Product
Phentermine, USP Capsules, 15 mg, 30 count bottles, Rx only, Packaged By: Aidarex Pharmaceuticals, Corona, CA, MFG: KVK-TECH INC. Newtown. PA --- 33261-0361-30
Reason for recall
Failed Impurities/Degradation Specification; out-of-specification results for individual unknown impurities at the 30 month Room Temperature Retained Sample stability 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-1162-2017. 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.