Philips Medical Systems Nederlands Recall: SmartPath to dStream for XR and 3.0T, Model Num

Name: Philips Medical Systems Nederlands Recall: SmartPath to dStream for XR and 3.0T, Model Num
Creator: RecallGuard

Philips Medical Systems Nederlands Recall: SmartPath to dStream for XR and 3.0T, Model Num is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Philips Medical Systems Nederlands; Product: SmartPath to dStream for XR and 3.0T, Model Number 781270. Nuclear Magnetic Resonance Imaging System;

Recalling firm	Philips Medical Systems Nederlands
Product	SmartPath to dStream for XR and 3.0T, Model Number 781270. Nuclear Magnetic Resonance Imaging System
Reason for recall	There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
Classification	Class II (moderate — may cause temporary or reversible health consequences)
Status	Terminated
Distribution	U.S. Nationwide distribution.
Recall initiated	20181221
Recall number	Z-0903-2019
Category	device
Country	Netherlands

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