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

Recall Z-1086-2025 — AlluraXperFD20/15 System Code: (1) 722058

U.S. FDA — Device Enforcement · Netherlands · 2025-01-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1086-2025
Date of alert
2025-01-13
Country / jurisdiction
Netherlands
Risk level
Class II
Risk type
recall
Brand
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00884838059115
Reported risk: Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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