Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0349-2023 — A. MENARINI diagnostics Hb 9210 PREMIER, LEVEL1, LEVEL II, Hemoglobin A1c Controls for hemoglobin A1c Assay, REF 45052, part number 05-01-0926, A1c analysis

U.S. FDA — Device Enforcement · United States · 2021-10-05 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0349-2023
Date of alert
2021-10-05
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Primus Corporation dba Trinity Biotech
Product category
device
Product type
Devices
Reported risk: The Control Level I material value was showing results exceeding the upper limit of the acceptable range after a period of three (3) months. The unacceptable Control Level 1 value results in the Analyzer generating an error code which stops further testing and nullifies associated patient samples, resulting in a delay in patient results and a potential delay in therapeutic modifications.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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