Class II — Beckman Coulter, Inc.
| Recalling firm | BECKMAN COULTER, INC. |
|---|---|
| Registered facility | View this company's 22 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics |
| Product | MicroScan Neg MIC 3J REF C54814 |
| Quantity | 688 boxes (20 panels per box) |
| Distribution | International distribution in the country of Japan. |
| Initiated | 2025-06-25 |
| Classified | 2026-04-03 |
| Recall number | Z-1772-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Beckman Coulter, Inc. (Z-1772-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98553/
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