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 RK040A - Kits f⁠rom lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.

Source: FDA | Recall date: 05/20/2026

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

Summary: Kits f⁠rom lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.

Hazard: Kits f⁠rom lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.

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