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

Recall Z-1586-2023 — Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72813

U.S. FDA — Device Enforcement · United States · 2023-03-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1586-2023
Date of alert
2023-03-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips North America
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00884838085015
Reported risk: Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload Pedal of the foot switch to perform the unload function may cause entrapment of the operator's foot and 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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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.