The FDA issued a notice to label a recall of Johnson & Johnson MedTech's Cerenovus unit's detachable coils as its most ...
A fault in J&J MedTech’s CEREPAK detachable coils, used in intracranial aneurysm embolisation procedures, has been associated ...
The FDA has flagged J&J Medtech’s recall of its Cerepak detachable coils as Class I in the wake of one death and four serious ...
FDA escalates Johnson&Johnson brain coil recall to Class I after device failures linked to patient death and serious injuries ...
J&J MedTech recalls neuro device following four injuries and one death linked to detachment failures in Cerepak coil systems.
Healthcare providers are advised to stop using the devices after a failure to detach was linked with four serious injuries ...
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