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

Recall Z-2179-2017 — Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems

U.S. FDA — Device Enforcement · United States · 2017-02-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2179-2017
Date of alert
2017-02-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
GE Healthcare, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
0910083012
Reported risk: Reported incidents of a patient step detaching from the table. A fall from a patient step detaching while in use could result in an injury to a patient or operator.
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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