Aniara Diagnostica LLC
4
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-05-20 to 2026-08-12
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-08-12 | FDA Device | FDA Recall: 5-PLASMA Bivalirudin Control, Model Number 5D-44905 | Aniara Diagnostica LLC | Class II | N/A |
| 2026-08-12 | FDA Device | FDA Recall: 5-PLASMA Bivalirudin AMR Verification Kit, Model Number 5D-45905 | Aniara Diagnostica LLC | Class II | N/A |
| 2026-08-12 | FDA Device | FDA Recall: 5-PLASMA Bivalirudin Calibrator, Model Number 5D-46905 | Aniara Diagnostica LLC | Class II | N/A |
| 2026-05-20 | FDA Device | FDA Recall: ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A | Aniara Diagnostica LLC | Class II | N/A |