The anatomy of vertebrobasilar perforators has been widely studied in human cadavers, with most reports found in the neurosurgical literature. These arterial perforators are extremely hard to ...

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

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

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

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

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 ...

Dive Brief: Integra Lifesciences has recalled cranial drills over a defect linked to 10 injuries, the Food and Drug Administration said Wednesday. The company has asked customers to return Codman ...