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 ...
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 ...
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.
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.
Pharmabiz

Balt’s Squid liquid embolic receives US FDA approval for adjunctive treatment for chronic subdural hematomas

Balt’s Squid liquid embolic receives US FDA approval for adjunctive treatment for chronic subdural hematomas: Boston Friday, February 6, 2026, 17:00 Hrs [IST] Balt Inc, a global ...
Newspoint on MSN

Brain hemorrhage: Why does it happen? Learn from experts its causes, types, and the most important prevention methods.

Causes of Brain Hemorrhage: A brain hemorrhage is an emergency situation that can be fatal if the patient does not receive timely treatment. Let us explain its symptoms. Brain haemorrhage Early Signs ...