Beckman Coulter Biomedical GmbH
1
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-08-12 to 2026-08-12
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-08-12 | FDA Device | FDA Recall: REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Info REMISOL A | Beckman Coulter Biomedical GmbH | Class II | N/A |