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

Recall Z-0694-2019 — Ingenia Elition S, Ingenia Elition X

U.S. FDA — Device Enforcement · Netherlands · 2018-12-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0694-2019
Date of alert
2018-12-03
Country / jurisdiction
Netherlands
Risk level
Class II
Risk type
recall
Brand
Philips Medical Systems Nederlands
Product category
device
Product type
Devices
Reported risk: During automatic tabletop movement, pressing and holding the Stop Table button may lead to an unexpected restart of the table movement.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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