Abbott Recalls HeartMate LVAS For Obstruction Issue
Abbott is recalling its HeartMate II and 3 LVAS due to Extrinsic Outflow Graft Obstruction, which can lead to severe health risks or death.
Read MoreAbbott is recalling its HeartMate II and 3 LVAS due to Extrinsic Outflow Graft Obstruction, which can lead to severe health risks or death.
Read MoreScott Lucas, PhD, PE, vice president of device safety at ECRI, talks about how skin tone affects pulse oximeters and racial inequity in healthcare.
Read MoreApr 10, 2024 | Ventilators | 0 |
A consent decree of permanent injunction was issued against Philips Respironics, halting production of their sleep therapy devices.
Read MoreTeleflex is recalling the Arrow QuickFlash Radial Artery and Radial Artery/Arterial Line Catheterization Kits after reports of issues.
Read MoreMar 29, 2024 | Infusion Therapy | 0 |
InfuTronix issued a voluntary recall of certain Numbus Ambulatory Infusion Pump Systems due to a high number of complaints.
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