Tri-Mix 18/1/10 — Class II drug recall D-0004-2017
Terminated recall by The Apothecary Shoppe LLC, reported 2016-10-12, distributed in OK. Lack of Assurance of Sterility; medication was sterilized with a recalled filter
| Recall number | D-0004-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Apothecary Shoppe LLC, Tulsa, OK, United States |
| Recall initiated | 2016-09-12 |
| Classified | 2016-10-04 |
| Reported by FDA | 2016-10-12 |
| Terminated | 2018-01-25 |
| Distributed | OK |
| Quantity | 247.5 ml |
| Reason classes | sterility |
| Expiration dates | 2016-09-22, 2016-10-08 |
Product
Tri-Mix 18/1/10 (Papaverine 18mg, Phentolamine 1 mg, Prostaglandin 10 mcg/mL) packaged in 2.5 mL sterile vials, IM, Rx, The Apothecary Shoppe, Jenks, OK
Reason for recall
Lack of Assurance of Sterility; medication was sterilized with a recalled filter
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-0004-2017. 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.