MIC Injection USP — Class II drug recall D-1525-2014
Terminated recall by Medical Supply Liquidators Llc, reported 2014-08-13, distributed nationwide. Marketed without an Approved NDA/ANDA; IM and SQ injectable products are being recalled because the manufactur
| Recall number | D-1525-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Supply Liquidators Llc, Clive, IA, United States |
| Recall initiated | 2014-06-25 |
| Classified | 2014-08-06 |
| Reported by FDA | 2014-08-13 |
| Terminated | 2017-03-14 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, DE, ES, FI, GB, HR, SI |
| Reason classes | unapproved product |
Product
MIC Injection USP, Sterile, 10 ml vial and 30 ml vial, For IM or Deep SQ Use, Multiple Dose Vial, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us
Reason for recall
Marketed without an Approved NDA/ANDA; IM and SQ injectable products are being recalled because the manufacturing firm is not registered with the FDA as a drug manufacturer
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-1525-2014. 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.