Philips’ Ventilator Woes Drag on with Yet Another Class I Recall
The U.S. FDA announced a Class I recall—the most serious type of recall—for the Philips Respironics V60 and V60 Plus Ventilator.
Read More
Search Results for: recall
Cybellum Joins Health-ISAC Navigator Program
Cybellum will share best practices with the Health-ISAC Community on the quick detection of device vulnerabilities and security risk posture.
Read More
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.
Read More
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.
Read More
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.
Read More