BD KIESTRA LAB AUTOMATION
1
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-04-08 to 2026-04-08
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-04-08 | FDA Device | FDA Recall: BD Kiestra" ReadA; Catalog No.: 446948. | BD KIESTRA LAB AUTOMATION | Class II | N/A |