Medical device recall events in 2024 reached their highest level since 2020 and more than 10% of them involved the most serious type of recall. There were 1,048 medical device recalls in 2024 ...
In 2016, medical device giant Abbott issued a recall for its MitraClip cardiac device — "a Class I recall, the most serious type," the FDA said. "Use of this device may cause serious injuries or ...
The recall, which affects two models of Pipeline Vantage embolization devices, is linked to 17 injuries and four deaths.
A new study found that 9.1% of medical device AEs were reported to the FDA 180 days later than required over a three-year period.
Over 16,000 units of Woolite Delicates laundry detergent were voluntarily recalled by the brand after it was discovered that ...
Bausch + Lomb has reported a “voluntary recall” of certain intraocular lenses (IOLs) on its enVista platform due to complications.
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: ...
Here are some of the latest recalls reported to the FDA ... providers have been advised to discontinue the use of affected devices immediately and return them to Olympus. There have been 26 ...
The US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as ...
The FDA deemed a recall of some Medtronic Pipeline Vantage embolization devices serious after multiple deaths related to the ...
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But in the world of medical devices ... has a wealth of information about device safety warnings, complaints, and recalls, easily accessible by typing the name of the device into the site's ...