MedTech Dive

J&J recalls coil systems used in aneurysm treatment

Healthcare providers are advised to stop using the devices, after a failure to detach was linked with four serious injuries ...
GlobalData on MSN

FDA classifies J&J MedTech’s CEREPAK recall as Class I following patient death

A fault in J&J MedTech’s CEREPAK detachable coils, used in intracranial aneurysm embolisation procedures, has been associated ...
TheHealthSite

Sudden Numbness Can Be A Sign Of Brain Aneurysm: Here's What You Need To Know

Numbness may be an early sign of an aneurysm of the brain.Here's what you should be knowing about the symptoms, causes, risk ...
MassDevice

FDA says recall of J&J’s Cerenovus detachable coils is serious

The FDA issued a notice to label a recall of Johnson & Johnson MedTech's Cerenovus unit's detachable coils as its most serious kind.

Centennial coach Zach Hettel's life-threatening event changed outlook

Zach Hettel, who was once one of the more fiery high school basketball coaches, has become more patient. Nearly dying will do ...
Becker's Hospital Review

J&J MedTech recalls neuro device after 4 injuries, 1 death

J&J MedTech recalls neuro device following four injuries and one death linked to detachment failures in Cerepak coil systems.
Stevens Point Journal

Chinese Neurosurgical Journal Study Shows Neuroform Atlas Stent-Assisted Coiling is Effective Even in Smaller Arteries

Neuroform Atlas stent-assisted coiling yields favorable outcomes in treatment of intracranial aneurysms in arteries less than 2.5 mm in diameter BEIJING, BEIJING ...