SIU-Tri-Mix 24/1/20 Injection — Class II drug recall D-1307-2015
Terminated recall by The Apothecary Shoppe LLC, reported 2015-08-12, distributed in OK. Lack of Assurance of Sterility: Due to lack of documentation of proper environmental monitoring during the tim
| Recall number | D-1307-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Apothecary Shoppe LLC, Tulsa, OK, United States |
| Recall initiated | 2015-06-26 |
| Classified | 2015-08-06 |
| Reported by FDA | 2015-08-12 |
| Terminated | 2017-02-17 |
| Distributed | OK |
| Quantity | 5 ml |
| Reason classes | sterility |
| NDC | 13861-1747-39 |
| Expiration dates | 2015-11-01 |
Product
SIU-Tri-Mix 24/1/20 Injection, Rx Only, 5 mL Vial, Apothecary Shoppe, Compounding Pharmacy, Tulsa OK 74135, NDC 13861-1747-39
Reason for recall
Lack of Assurance of Sterility: Due to lack of documentation of proper environmental monitoring during the time in which the medication was produced.
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-1307-2015. 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.