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

Recall Z-2310-2016 — AU5800 Chemistry Analyzers, Reference No. A98352 The AU series are automated, clinical chemistry analyzers that measure analytes in patient samples (serum, plasma, urine, CSF) in combination with appropriate reagents, calibrators, quality, control (QC) materials, and other accessories.

U.S. FDA — Device Enforcement · United States · 2015-07-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2310-2016
Date of alert
2015-07-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Beckman Coulter Inc.
Product category
device
Product type
Devices
Reported risk: Beckman coulter has received complaints regarding leaking and cracked C cups. When the cup cracks, coolant can leak onto the connectors of the Printed Circuit Boards (PCB) in the analyzer, resulting in a short-circuit causing the instrument to go into a stop mode.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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