Accriva Diagnostics, Inc.
1
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-06-24 to 2026-06-24
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-06-24 | FDA Device | FDA Recall: directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2 | Accriva Diagnostics, Inc. | Class II | N/A |