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

Recall Z-1806-2020 — Philips TraumaDiagnost- a Stationary X-Ray System (Bucky System) Model: 720013 - Product Usage: general radiography.

U.S. FDA — Device Enforcement · United States · 2020-04-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1806-2020
Date of alert
2020-04-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips North America, LLC
Product category
device
Product type
Devices
Reported risk: If the shaft breaks due to material fatigue, the trauma arm can fall down and may result in injury.
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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