Testosterone 200 mg pellet packaged in amber vial — Class II drug recall D-0662-2018
Terminated recall by Partell Specialty Pharmacy, reported 2018-04-25, distributed in NV. Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of steriliza
| Recall number | D-0662-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Partell Specialty Pharmacy, Las Vegas, NV, United States |
| Recall initiated | 2018-03-22 |
| Classified | 2018-04-17 |
| Reported by FDA | 2018-04-25 |
| Terminated | 2019-01-15 |
| Distributed | NV |
| Reason classes | sterility |
| Expiration dates | 2018-04-08, 2018-04-17, 2018-04-29, 2018-05-01, 2018-05-09, 2018-05-13, 2018-05-21, 2018-05-27, 2018-05-30, 2018-06-09, 2018-06-16, 2018-06-20, 2018-07-11, 2018-07-15, 2018-07-21, 2018-08-01, 2018-08-04, 2018-08-08, 2018-08-11, 2018-08-18, 2018-08-22 |
Product
Testosterone 200 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3
Reason for recall
Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
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-0662-2018. 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.