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Sorin Group Deutschland Recalls
4 recalls on record · November 13, 2013 to January 31, 2018 · Medical Devices
Recalls by year
13
14
18
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
January 31, 2018Medical DevicesFDA
Sorin Group Deutschland GmbH recalls CP5 Centrifugal Pump, made up of the drive unit, the emergency system and the pump control panel. It used with an Elect
Hazard: Possibility that the automatic line closure by the Electronic Remote-Controlled (ERC) clamp after detection of an air bubble could take longer than is intended by design in the CP5 system.
February 5, 2014Medical DevicesFDA
Sorin Group Deutschland GmbH recalls CP5 centrifugal pump system Product Usage: The Stockert S5/ Sorin C5 System is intended to be used during cardiopulm
Hazard: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5 centrifugal pump system due to reports of pump speed control knob failures resulting in no response.
February 5, 2014Medical DevicesFDA
Sorin Group Deutschland GmbH recalls S5/C5 Heart-lung machine Product Usage: The StOckert S5/ Sorin C5 System is intended to be used during cardiopulmona
Hazard: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5 centrifugal pump system due to reports of pump speed control knob failures resulting in no response.
November 13, 2013Medical DevicesFDA
Sorin Group Deutschland GmbH recalls S5 Heart-lung machine, Stockert S5 System. Catalogue No: 48-30/40/50-00. The Stockert S5 System is intended to be us
Hazard: Sorin Group is recalling certain models of S5 Perfusion Systems due to malfunction of cardioplegia control.