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Medtronic Removes Tracheostomy Tube Over Risk of Flange Disconnection

Medtronic advises customers to return affected adult flexible tubes due to potential airway blockage and respiratory emergencies.

GE HealthCare has issued an update to the EVair Compressor recall, with testing results confirming safe usage across all patient groups.

Medline recalled the Sub-G Endotracheal Tube with Subglottic Suction due to risks of detachment, tearing, and potential airway obstruction.

Medtronic advises customers to return affected adult flexible tubes due to potential airway blockage and respiratory emergencies.

Apr 16, 2024

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

Apr 15, 2024

Abbott is recalling its HeartMate II and 3 LVAS due to Extrinsic Outflow Graft Obstruction, which can lead to severe health risks or death.

Apr 10, 2024

A consent decree of permanent injunction was issued against Philips Respironics, halting production of their sleep therapy devices.

Apr 4, 2024

Teleflex is recalling the Arrow QuickFlash Radial Artery and Radial Artery/Arterial Line Catheterization Kits after reports of issues.

Mar 22, 2024

Vyaire Medical is recalling certain AirLife Manual Resuscitators due to a life-threatening manufacturing defect.

Feb 9, 2024

Philips has recalled its BrightView SPECT imaging systems for a potential component failure that would cause parts to fall on the patient.

Philips announced that it would stop selling CPAP or BiPAP sleep therapy devices and other respiratory care devices in the U.S.