Cracked, Broken Power Switches Lead To Class I Recall For Getinge Anesthesia Systems
The US FDA gave a high-risk class I designation to a recall of Getinge’s Flow-c and Flow-e systems.
You may also be interested in...
In this FINAL EPISODE of Speaking Of Medtech: The US FDA got something it desperately wanted in its latest user-fee package with industry: a Total Product Lifecycle Advisory Program pilot, or TAP. The agency says TAP will allow for earlier and more frequent engagement with developers – but is it needed?
People with obesity now have new tools to help them lose weight, thanks to the US agency’s de novo authorization.
More than 160,000 of the tests were recalled, including 104,900 COVID Test Kits Nonsterile and 61,500 Clean Catch Urine Kits.