Medical device recalls Moderate risk

TECHNO-PATH MANUFACTURING LTD. recalls Multichem ID-B. Model Number: SR103B. Intended for use as an unassayed positive qualitative quality control serum to mo…

Recall date
October 17, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0502-2026
FDA classification
Class II
Brand / firm
TECHNO-PATH MANUFACTURING LTD.
Sold / distributed
US distribution to CA, CO, CT, FL, HI, IL, LA, MI, MN, NV, NY, OR, SC, TN, TX, WI, WY.

Why it was recalled

Potential of negative recovery of the HBsAg analyte across two (2) lots of Multichem ID-B Positive Control when tested on the Alinity i platform.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Multichem ID-B. Model Number: SR103B. Intended for use as an unassayed positive qualitative quality control serum to monitor the precision of laboratory testing procedures for the determination of anti-HIV-1 IgG, anti-HBc IgG, anti-HTLV-I IgG, anti-HCV IgG, HBs antigen and anti-Treponema pallidum IgG.

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