FDA recall record

Philips Medical Systems Nederlands SmartPath to dStream for XR and 3.0T, Model Number 781270 recall — FDA Z-0903-2019

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.

Class IIclassification
Z-0903-2019official record ID
Mar 6, 2019report date

Recall record at a glance

Official recordZ-0903-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPhilips Medical Systems Nederlands
Report dateMar 6, 2019
Recall initiation dateDec 21, 2018
Quantity11226 total
LocationBest, Netherlands

Official product description

SmartPath to dStream for XR and 3.0T, Model Number 781270. Nuclear Magnetic Resonance Imaging System

Why the product was recalled

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.

Distribution information

U.S. Nationwide distribution.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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