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FDA (Device enforcement)Recalled 2023-03-01class ii

Terumo Cardiovascular Systems Corporation: CAPIOX NX19 Hollow Fiber Oxygenator, Catalog Number 3CX*NX19RE

Hazard

Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor component that is improperly bonded to the oxygenator port. This may result in a leak at the point where the arterial thermistor is improperly bonded to the oxygenator port.

Details from the source

Reason for recall: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor component that is improperly bonded to the oxygenator port. This may result in a leak at the point where the arterial thermistor is improperly bonded to the oxygenator port. Distribution: US Nationwide. Belgium, Canada, Costa Rica, Thailand. Quantity: 84 units Lot/code info: UDI-DI: (01)00699753450868; Lot Number AM03

UPC codes

00699753450868

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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