Earlier this year, Abbott recalled the HeartMate II and HeartMate 3 systems due to a graft obstruction problem that, as of ...

Only a week after Neuralink disclosed that its first patient implanted with the device was experiencing the tiny threads in ...

An investigative news report exposes a significant flaw in the regulatory system: FDA oversight relies heavily on ...

The agency continues to recommend healthcare providers use syringes not manufactured in China after reports of leaks, ...

The F15 recharge-free sacral neuromodulation system is indicated for the treatment of adults with overactive bladder.

The recall, which was initiated by the company in March, pertains to a software issue that can cause a possible power ...

Masimo recently announced the recall of some of its Rad-G pulse oximeters after reports of unintended change of device power ...

A separation of Masimo's consumer business from its core healthcare business seems to have provided a light at the end of its ...

Magadyne reported it has received four reports of injury and no reports of death associated with the recall since 2018.

Myotronics became embroiled in a fight with FDA that ultimately led to disciplinary action against two agency employees and ...

This week in Pedersen's POV, our senior editor shares slacker-inspired tips for beating mandatory training procrastination ...

Deemed a correction, not product removal, the company is urging customers to update the apps software to mitigate potential ...