Bimix — Class II drug recall D-1120-2015
Terminated recall by Montana Compounding Pharmacy, reported 2015-06-17, distributed in MT, ND. Lack of Assurance of Sterility; objectionable conditions observed during a FDA inspection
| Recall number | D-1120-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Montana Compounding Pharmacy, Missoula, MT, United States |
| Recall initiated | 2015-05-15 |
| Classified | 2015-06-09 |
| Reported by FDA | 2015-06-17 |
| Terminated | 2016-12-20 |
| Distributed | MT, ND |
| Quantity | 1 |
| Reason classes | sterility |
| Expiration dates | 2015-07-03 |
Product
Bimix (PHENT;PAP) (N), solution, (10/300) 1 - 30 mg/mL, injectable, 5ml vial, Rx only, compounded by Montana Compounding Pharmacy in Missoula, MT.
Reason for recall
Lack of Assurance of Sterility; objectionable conditions observed during a FDA inspection
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-1120-2015. 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.