AirLife and Vyaire are recalling specific infant breathing support systems due to a potentially dangerous defect that could ...

Using recalled AirLife Infant Heated Wire Circuits could cause cause carbon dioxide build up in the blood, a lack of oxygen ...

Medical device recalls 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: Airlife and Vyaire ...

None of the items were made by Amazon, but they were available via its website until the retailer became aware of the recalls. Amazon subsequently contacted its affected customers and publicized the ...

The FDA issued a notice identifying a high-risk device issue associated with a Medtronic recall of Bravo CF capsule delivery devices.

An urgent recall has gone out for a popular medical devices used by millions of Americans dealing with a chronic health condition.

Receiving a recall notice for a medical device can be deeply unsettling for Louisiana residents who rely on these devices daily—whether for sleep support, pain management, or mobility—news of ...

FDA classifies recall of Medtronic embolization devices as 'most serious' The recall impacts the Pipeline Vantage devices compatible only with 0.027" inner diameter microcatheters, Medtronic said ...

My firm’s recent 2024 Recall Report further suggests an alarming disconnect between consumer concerns about medical product safety and their actions when faced with recalls. We found that just ...

Meeting Coverage > STS Limbo of Cardiac Device Recalls Has Physicians Ready for Change — How innovation may play out under Trump, and medicolegal implications of using recalled devices by Nicole ...

Recalled heart devices often do not go through clinical testing, a new study found, highlighting growing concerns about the FDA’s medical device approval standards.

The FDA and manufacturers routinely allow doctors and hospitals to continue using medical devices that could cause serious harm or death.