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

Recall Z-1146-2025 — Allura Xper FD20 Biplane OR Table; Catalog numbers: (1) 722020, (2) 722025.

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

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1146-2025
Date of alert
2025-01-13
Country / jurisdiction
Netherlands
Risk level
Class I
Risk type
recall
Brand
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00884838059108
Reported risk: Possibility of the patient falling from the table related to the mattress used on the patient table.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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