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

Recall Z-0154-2020 — Viva - JR, catalog # 6002-940, UDI # 03661540600210 Product Usage: automated chemistry analyzer intended for clinical use

U.S. FDA — Device Enforcement · Netherlands · 2012-01-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0154-2020
Date of alert
2012-01-10
Country / jurisdiction
Netherlands
Risk level
Class II
Risk type
recall
Brand
Vital Scientific N.V.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
03661540600210
Reported risk: The action was initiated due power supply failure. During a power supply failure the instruments malfunctions and no patient results are produced.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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