MassDevice3d
Medline has a Class I arterial catheter recall
The FDA labeled a recall of integrated arterial catheters made by Medline Class I, the most serious kind of recall.
dvm3604d
FDA notifies veterinarians of animal burn risk linked to human medical devices
Following a recall of grounding pads produced by Megadyne, a machinery industry company, the FDA is notifying veterinarians ...
The New Yorker2d
My Life with Left-Handed Women
Waiting for them under the tree in our sunny Pasadena living room might be left-handed oven mitts or can openers, kitchen ...
Canada5d
Pre-market guidance for machine learning-enabled medical devices
Manufacturers should clearly state that the device uses ML in their cover letter ... example, performance envelope) and how the changes will be implemented and assessed. The changes described in a ...
Becker's Hospital Review3d
4 recent medical device recalls and corrections
JIANGSU JUMAO X-CARE Medical Equipment Co. issued a recall for the JMC5A Ni/Tru-Aire-5 Oxygen Concentrator after incidents of spontaneous fires. These fires could cause burns or worse. Patients are ...
medtechdive4d
FDA labels recall of discontinued Olympus endoscope part as Class I
The update comes about six weeks after an early alert flagged reports of 120 injuries and one death linked to reprocessing of ...
TCTMD3d
FDA Issues Early Alert About Risks of Peripheral Atherectomy Device
Fractures and breakages of the helix on the Rotarex system has led to 30 serious injuries, four deaths, and 115 interventions ...
St. Louis Post-Dispatch4d
Letter: Donald Trump's attack on WHO and U.S. medical info is irresponsible
*Refers to the latest 2 years of stltoday.com stories. Cancel anytime. As a physician of 40 years experience, I cannot believe the folly of the past two weeks. Avian influenza ("bird flu") is ...