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

Recall Z-2573-2018 — Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-540

U.S. FDA — Device Enforcement · United States · 2018-01-05 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2573-2018
Date of alert
2018-01-05
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Diamedix Corporation
Product category
device
Product type
Devices
Reported risk: Contains a gel-like contaminant that may affect product performance.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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