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

Recall Z-2494-2012 — Philips Digital Diagnost with patient carriage Model: 712050 with serial number range from 00 000 00 to 09 000 543. Product Usage: Stationary radiographic System

U.S. FDA — Device Enforcement · United States · 2012-09-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2494-2012
Date of alert
2012-09-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips Healthcare Inc.
Product category
device
Product type
Devices
Reported risk: Hook does not securely hold the footplate in vertical position, causing the footplate to disengage and may fall on patient or operator
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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