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Maquet Cardiovascular Us Sales Recalls
62 recalls on record · July 18, 2012 to December 23, 2020 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 7, 2012Medical DevicesFDA
Maquet Cardiovascular Us Sales, Llc recalls QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator; QUADROX-i ADULT HMO 70000 / HMO 71000; QUADROX-iD Pediatric HMOD 300
Hazard: It has come to firm's attention that, in some rare cases, the blood outlet connector on some models of MAQUET Oxygenators may detach from the oxygenator. This event has occurred in about 0.01% (1:10,000) of units shipped.
July 18, 2012Medical DevicesFDA
Maquet Cardiovascular Us Sales, Llc recalls FLOW-I Anesthesia System The system is intended for use in administrating anesthesia while controlling the entire ven
Hazard: A technical alarm may be generated on the FLOW-i system when using the MAN/AUTO switch to change ventilation modes from manual to automatic or from automatic to manual if the switch is not fully engaged in the "on" or "off" position but remains in the "in-between position.