Smiths Medical Recalls PneuPac paraPAC Plus Ventilator Kits
Smiths Medical is recalling its paraPAC Plus 300 and 310 Ventilator Kits due to a malfunction where the device may not cycle properly.
Read MoreSmiths Medical is recalling its paraPAC Plus 300 and 310 Ventilator Kits due to a malfunction where the device may not cycle properly.
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.
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