Drug recall
MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212 MicroScan panels are designed for use in…
FDA recall event 98555 · Class II · Beckman Coulter, Inc.
Key facts
| Event ID | 98555 |
|---|---|
| Recall numbers | Z-1609-2026 |
| Recalling firm | Beckman Coulter, Inc. |
| Product type | Devices |
| Products | MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212 MicroScan panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Due to the likely presence of contamination in well(s). |
| Initiation date | Jul 24, 2025 |
| Report date | Apr 1, 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: