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Medical Device

ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A

Recall date: 2026-05-20 · Source: FDA_DEVICE
Brand / Firm
Aniara Diagnostica LLC
Product
ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A
Reason for recall
Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.
Units affected
359 units
Description
ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A
View official recall notice →