PlainRecalls
FDA Devices Moderate Class II Terminated

Prodiva CS, Model Number 781069. Nuclear Magnetic Resonance Imaging System

Reported: March 6, 2019 Initiated: December 21, 2018 #Z-0869-2019

Product Description

Prodiva CS, Model Number 781069. 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.

Details

Units Affected
11226 total
Distribution
U.S. Nationwide distribution.
Location
Best

Frequently Asked Questions

What product was recalled?
Prodiva CS, Model Number 781069. Nuclear Magnetic Resonance Imaging System. Recalled by Philips Medical Systems Nederlands. Units affected: 11226 total.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 6, 2019. Severity: Moderate. Recall number: Z-0869-2019.