Philips Medical Systems Nederlands recalls Multiva 1.5T 16 R5 (ZBO), Model Number 781073. Nuclear Magnetic Resonance Imaging System
- Recall date
- December 21, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0872-2019
- FDA classification
- Class II
- Brand / firm
- Philips Medical Systems Nederlands
- Sold / distributed
- U.S. Nationwide distribution.
Why it 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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Multiva 1.5T 16 R5 (ZBO), Model Number 781073. Nuclear Magnetic Resonance Imaging System
Get recall alerts
Free email alert whenever Philips Medical Systems Nederlands has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Philips Medical Systems Nederlands