FDA Upgrades Baxter Infusion Pump Safety Issue to Class I Recall
Baxter International has issued a Class I recall—the most serious type of recall—for its its Spectrum V8 and Spectrum IQ infusion pumps.
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Search Results for: recall
Medtronic Recalls TurboHawk Plus Atherectomy System
Medtronic is recalling a directional atherectomy system, which is used during procedures intended to remove blockage from peripheral arteries.
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FDA Orders Philips to Notify Patients of Recall of Certain Breathing Assistance Machines
The FDA issued a notification order to Philips Respironics requiring the company to of the recall of certain breathing assistance machines.
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Clinical Asset Management Strategies
Many hospital administrators are spending more money than necessary on clinical assets. This isn’t to say that they are intentionally wasting money. They’re not. But when it comes to buying medical devices, a host of factors can make savvy purchasing challenging.
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FDA Urges Companies to Be ‘Recall Ready’ to Protect Public Health
The FDA finalized guidance to help companies prepare to quickly and effectively remove violative products from the market.
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