TRIMIX — Class II drug recall D-0152-2016
Terminated recall by JD & SN Inc., dba Moses Lake Professional Pharmacy, reported 2015-11-04, distributed nationwide. Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
| Recall number | D-0152-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | JD & SN Inc., dba Moses Lake Professional Pharmacy, Moses Lake, WA, United States |
| Recall initiated | 2015-07-24 |
| Classified | 2015-10-27 |
| Reported by FDA | 2015-11-04 |
| Terminated | 2016-04-13 |
| Distributed | Nationwide (US) |
| Quantity | 3 syringes |
| Reason classes | sterility |
Product
TRIMIX, injectable Solution, 40MG/2MG/40MCG/ML, syringe size: 10mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
Reason for recall
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
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-0152-2016. 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.