Dextrose* Vial In Sterile Water — Class I drug recall D-1156-2014
Terminated recall by Specialty Medicine Compounding Pharmacy, P.C., reported 2014-03-19, distributed in MI. Non-Sterility: 50% dextrose is being recalled after particulate matter, later identified as mold, was found fl
| Recall number | D-1156-2014 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Specialty Medicine Compounding Pharmacy, P.C., South Lyon, MI, United States |
| Recall initiated | 2013-10-19 |
| Classified | 2014-03-12 |
| Reported by FDA | 2014-03-19 |
| Terminated | 2014-09-22 |
| Distributed | MI |
| Quantity | 1,000 vials |
| Reason classes | microbial contamination, sterility, specification failure |
| Pathogens | mold |
| Expiration dates | 2013-10-20, 2013-10-21, 2013-10-23, 2013-10-28, 2013-11-03, 2013-11-07, 2013-11-10, 2013-11-14, 2013-11-17 |
Product
Dextrose* Vial In Sterile Water, 50%, 50 mL Single Dose Vial, Rx only, Specialty Medicine Compounding Pharmacy, 350 S Lafayette, South Lyon, MI 48178
Reason for recall
Non-Sterility: 50% dextrose is being recalled after particulate matter, later identified as mold, was found floating in the product.
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-1156-2014. 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.