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Ventilator recall issued with warning of "serious injuries or death"
Newsweek· 14 hours agoTrilogy EVO, Trilogy EV300, Trilogy Evo O2, and Trilogy Evo Universal—have been assigned a Class I ...
FDA Recalls Insulin Pump App After 200+ Injuries
Verywell Health via Yahoo News· 14 hours agoTandem Diabetes Care Fact checked by Nick Blackmer Key Takeaways The FDA is recalling an insulin pump app. The t:connect mobile app may drain the battery...
Chia Seeds Have Been Recalled Nationwide Due to Possible Salmonella Contamination—Here's What You...
Martha Stewart Living via Yahoo News· 14 hours agoWalmart The recall affects some 32-ounce bags of Great Value Organic Black Chia Seeds. The products...
Aldi recalls cream cheese spread sold in 28 states for possible salmonella contamination
CBS News via Yahoo News· 15 hours agoA string of recalls connected to Wisconsin-based supplier Schreiber Foods has now extended to Aldi...
Philips' (PHG) Gets FDA Recall for Trilogy Ventilator Glitch
Zacks via Yahoo Finance· 1 day agoPhilips' (PHG) software update for Trilogy Evo ventilators is set to mitigate a possible power...
FDA issues recall notice for Philips after another respiratory device fails
Medical Device Network via Yahoo Finance· 18 hours agoThe FDA has issued the notice for the company’s Trilogy EVO Continuous Ventilators, warning that...
Over 877,000 Yogi Tea Bags Recalled Due To Elevated Levels of Pesticides
Simply Recipes via Yahoo News· 2 days agoThe FDA sets an "action level" for these unavoidable pesticides. If a product is found to have...
Recalled Snack Sold In Arizona Could Cause 'Life-Threatening' Reaction | iHeart
iHeartRadio· 21 hours agoA sweet snack sold around the country, including in Arizona, has been recalled after it was...
FDA elevates cardiovascular catheter recalls from Boston Scientific, Route 92 Medical
FierceBiotech· 1 day agoBoth companies’ efforts recently received Class I recall designations from the FDA, the agency’s...
After FDA warning, Getinge trims sales of heart devices
Becker’s Hospital Review· 21 hours agoThe decision is a response to the FDA's May 8 letter to providers, which said the agency has received 48 reports of deaths and serious injuries connected to Getinge balloon ...