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Recalls → Z-0206-2027
Class II Recall · Z-0206-2027 Report Date: 2026-10-28 · Status: Ongoing

TECHNO-PATH MANUFACTURING LTD. — Medical Devices Recall

Product Description: Techno-Path Multichem AE Unassayed Level 2 REF: AE622X
Reason for Recall: A routine stability studies have identified a stability drift affecting the Ammonia (NH4+) analyte in specific lots of Multichem AE quality control material. Additional testing confirmed that the labelled shelf-life performance claim for the Ammonia analyte can no longer be supported for the affected lots. This issue i
Distribution Pattern: US Nationwide distribution in the state of Massachusetts.
View Linked Facility Profile (FEI FEI-02BA1115) → Verify on openFDA ↗