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

Recall Z-0371-2019 — GE Healthcare Millennium MC

U.S. FDA — Device Enforcement · United States · 2018-09-14 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0371-2019
Date of alert
2018-09-14
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
GE Healthcare, LLC
Product category
device
Product type
Devices
Reported risk: A detector can detach and fall.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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