Aniara Diagnostica Recalls

1 recall found for Aniara Diagnostica. Check if any of your products are affected.

HIGH

FDA DEVICE

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

Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.

Apr 1, 2026

Aniara Diagnostica

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