TM #1 — Class II drug recall D-0645-2018
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-0645-2018 |
|---|---|
| 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 |
| Quantity | 15 vials |
| Reason classes | sterility |
| Expiration dates | 2018-03-29, 2018-04-02 |
Product
TM #1 (ALP 5.9/PAPAV 17.65/PHEN 0.59) Injectable solution, packaged in 3 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800
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-0645-2018. 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.