Medtronic, Baxter Face FDA Class I Labels for Separate Recalls of Heart Pumps, Ventilators
Amid continued recall concerns, devices from Medtronic and Baxter were recently assigned the most serious recall type be the FDA.
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BD Voluntarily Recalls Intraosseous Products
BD announced a voluntary recall on its Intraosseous Needle Set Kits, Intraosseous Manual Driver Kits, and Intraosseous Powered Drivers.
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Draeger Breathing Filter Gets Class I Recall
The Draeger SafeStar 55 has been identified by the U.S. FDA as a Class I recall, the most serious type of recall.
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‘This is Not a Good Situation’: Philips Engineer Flagged Ventilator Foam Issues Years Before Recall, Court Docs Show
A year after Philips initiated a safety recall of its ventilators, it was discovered that the company had long been aware of certain issues.
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Dräger’s Breathing System Filter Recall Gets Class I Label from FDA After Ventilation Obstruction
Dräeger Medical, Inc. expanded on its voluntary recall of Lot LT2103 of Draeger SafeStar 55 Breathing System Filters.
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