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Z-0932-2019 Class II Terminated

Recalled by Philips Medical Systems Nederlands — Best

Recall Details

Product Type
Devices
Report Date
March 6, 2019
Initiation Date
December 21, 2018
Termination Date
November 19, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
11226 total

Product Description

Multiva 1.5T, Model Number 781076. 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.

Distribution Pattern

U.S. Nationwide distribution.

Code Information

All systems

Other recalls by Philips Medical Systems Nederlands

  • Z-1240-2019 Class II — Ingenia Ambition S (781359), Ingenia Ambition X (781356) with Magnet Energizatio (March 25, 2019)
  • Z-1140-2019 Class II — Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product (February 19, 2019)
  • Z-1141-2019 Class II — Foot Switches used with the following systems: 722001 Allura Xper FD 10 C 72 (February 19, 2019)
  • Z-0920-2019 Class II — Ingenia Ambition S, Model Number 781359. Nuclear Magnetic Resonance Imaging Sy (December 21, 2018)
  • Z-0924-2019 Class II — MR-OR 1.5T, Model Number 781437. Nuclear Magnetic Resonance Imaging System (December 21, 2018)
  • Z-0918-2019 Class II — Ingenia 3.0T, Model Number 781377. Nuclear Magnetic Resonance Imaging System (December 21, 2018)
  • Z-0902-2019 Class II — Ingenia 1.5T CX (ZBO), Model Number 781262. Nuclear Magnetic Resonance Imaging (December 21, 2018)
  • Z-0893-2019 Class II — Achieva 3.0T, Model Number 781177. Nuclear Magnetic Resonance Imaging System (December 21, 2018)
  • Z-0870-2019 Class II — Prodiva CX, Model Number 781070. Nuclear Magnetic Resonance Imaging System (December 21, 2018)
  • Z-0887-2019 Class II — Intera Achieva 1.5T Pulsar, Model Number 781171. Nuclear Magnetic Resonance Im (December 21, 2018)