Drug recall
MicroScan Neg MIC 3J REF C54814
FDA recall event 98553 · Class II · Beckman Coulter, Inc.
Key facts
| Event ID | 98553 |
|---|---|
| Recall numbers | Z-1772-2026 |
| Recalling firm | Beckman Coulter, Inc. |
| Product type | Devices |
| Products | MicroScan Neg MIC 3J REF C54814 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics |
| Initiation date | Jun 25, 2025 |
| Report date | Apr 15, 2026 |
| City | West Sacramento |
| State | CA |
| Country | United States |
| FEI number | 2919016 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: