The FDA labeled a recall of integrated arterial catheters made by Medline Class I, the most serious kind of recall.
The update comes about six weeks after an early alert flagged reports of 120 injuries and one death linked to reprocessing of ...
The update comes about six weeks after an early alert flagged reports of 120 injuries and one death linked to reprocessing of the device.
What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.
Several executive orders recently signed by US President Donald Trump may have significant implications for the US Food and Drug Administration ...
The FDA has recalled Mercury Medical’s Neo-Tee T-Piece Resuscitator, a gas powered resuscitator intended primarily for ...
BIS issued an Interim Final Rule that amends the Export Administration Regulation (EAR) to address dual use export ...
The FDA is elevating a recall from Philips related ... we proactively identified a software configuration issue and reported a medical device correction, offering clinicians the possibility ...
Let's look at five pharma and drug companies, MRK PFE, LLY, AMGN and BMY, which are scheduled to release their fourth-quarter ...
ColdVentures enters exclusive distribution partnership with Medco Sports Medicine: Los Angeles Monday, January 27, 2025, 16:00 Hrs [IST] ColdVentures, a leading medical device com ...
A recent study identified 157 cardiovascular devices recalled from 2013 to 2022. Recalls were commonly attributed to device ...
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