The FDA is amplifying an effort underway at medical device distributor Medline that aims to correct certain neurosurgery kits ...

The defect has resulted in problems including a procedural delay, difficulty removing device fragments and bleeding, the FDA ...

The Food and Drug Administration has identified a Class I recall of certain lots of Medline Industries Craniotomy ...

If one looks closely, one can also see a small infarct in the right posterior thalamus. Small perforators from the proximal PCA supply the thalamus. In this case, the infarct was most likely caused by ...

The FDA issued a notice warning of an issue with certain Medline craniotomy kits due to an Integra LifeSciences perforator recall.

Between January 2005 and August 2015, the FDA received more than 300 medical device reports (MDRs) of automatic clutch mechanisms failing to disengage, resulting in more than 200 injuries, the ...

Medline has issued a correction for multiple craniotomy kits after reports of the devices disassembling during use. The recall affects several lot numbers of kits that include 14mm Codman disposable ...

Medical devices are essential to patient safety, addressing critical issues in devices that may pose health risks. Here are some of the latest recalls reported to the FDA: Integra LifeSciences has ...