News

American Hospital Association14h
FDA issues most serious recall for two Smiths Medical infusion pumps
The Food and Drug Administration issued Class I recalls, the most serious type, for two Smiths Medical infusion pumps due to ...
CNET17h
Set the Weights Down: BowFlex Adjustable Dumbbells Are Being Recalled. Here’s What to Know
Johnson Health Tech Trading has voluntarily recalled over 3.8 million sets of the BowFlex 552 and 1090 Adjustable Dumbbells.
MedTech Dive1d
Smiths Medical recalls infusion pumps over 3 problems
Smiths has not reported any serious injuries or deaths related to the issues, but the FDA sees a risk of harm.
American Hospital Association9d
FDA issues recall on tubes used to manage bleeding
The Food and Drug Administration has identified a Class I recall of certain lots of BD esophagogastric balloon tamponade ...
Modern Healthcare1mon
The companies with device recalls in Q1
Fewer medical devices were recalled during the first three months of the year, following a surge in recalls in 2024. In the first quarter of 2025, there were 708 medical device recalls ...
techtimes1mon
Microsoft Recall, AI Windows Search Now Rolling Out Again to Copilot+ PCs—Do Problems Still Exist?
In particular, the post elaborates on the return of AI Recall now rolling out to the aforementioned devices. Recall has seen almost 10 months of work from Microsoft, with the feature being ...
health.economictimes.indiatimes2mon
FDA classifies recall of Medtronic embolization devices as 'most serious'
Bengaluru: The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", following reports of the deaths of four patients. The use of ...
Seeking Alpha2mon
Medtronic slips after FDA notice on product recall (update)
The agency identified the recall as the most serious type. MDT’s Pipeline Vantage 027 devices are used to treat intracranial aneurysms. According to the FDA, the company has issued an urgent ...
Reuters2mon
FDA classifies recall of Medtronic embolization devices as 'most serious'
March 18 (Reuters) - The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's (MDT.N), opens new tab embolization device as "most serious", following reports of the ...
Becker's Hospital Review2mon
3 medical device recalls and corrections
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 ...
Modern Healthcare3mon
Medical device recalls hit a four-year high in 2024. Here’s why
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 ...
Monthly Prescribing Reference3mon
Boston Scientific Recalls Accolade Pacemaker Devices
The devices are being recalled due to an increased risk for permanently entering Safety Mode. HealthDay News — Boston Scientific has issued a recall of Accolade pacemaker devices, according to a ...