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

Recall Z-2120-2015 — GE Healthcare Precision 500D Classical R & F system.

U.S. FDA — Device Enforcement · United States · 2015-06-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2120-2015
Date of alert
2015-06-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
GE Healthcare
Product category
device
Product type
Devices
Reported risk: A reported incident of a monitor that fell from the suspension. A fall of a monitor could result in an injury to a patient or operator. Recall affects the single and dual LCD monitor suspensions used on Precision 500D Classical R & F system, Precision RXi 23A/32A Analog System, Precision RXi Digital system and Precision MPi fluoroscopic imaging systems.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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