Aniara Diagnostica LLC
1
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-05-20 to 2026-05-20
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-05-20 | FDA Device | FDA Recall: ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A | Aniara Diagnostica LLC | Class II | N/A |