MicroScan Neg MIC 3J REF C54814 — Class II medical device recall Z-1772-2026
Ongoing recall by Beckman Coulter, Inc., reported 2026-04-15. Due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics
| Recall number | Z-1772-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beckman Coulter, Inc., West Sacramento, CA, United States |
| Recall initiated | 2025-06-25 |
| Classified | 2026-04-03 |
| Reported by FDA | 2026-04-15 |
| Countries outside the US | JP |
| Model numbers | C54814 |
Product
MicroScan Neg MIC 3J REF C54814
Reason for recall
Due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics
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/Z-1772-2026. 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.