"Philips Recalls Panorama 1.0T HFO and Other Imaging Gear Due to Risk of Explosion"
TL;DR Summary
Philips North America is recalling its Panorama 1.0T HFO MRI system due to a risk of explosion during a quench procedure caused by excessive pressure buildup of helium gas. The recall affects 150 devices distributed in the U.S. between January 2001 and October 2016. The use of the affected system may result in serious injuries or death. Customers have been instructed to discontinue use, post warning notices, and contact Philips for inspection and repairs. There has been one reported event of an explosion in 22 years of use, with no reports of injury or death.
- Philips North America LLC Recalls Panorama 1.0T HFO due to a Risk of Explosion During a Quench Procedure Caused by Excessive Pressure Buildup of Helium Gas FDA.gov
- US FDA identifies recall of Philips medical imaging devices as most serious Reuters
- Philips Recalls Medical Imaging Gear on Risk of Explosion Bloomberg
- FDA announces Class I recall of 150 MRI scanners due to risk of explosion Health Imaging
- Philips recalls some imaging machines on explosion concerns Yahoo Finance
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