Z-1347-2023 Class II Ongoing

Recalled by Terumo Cardiovascular Systems Corporation — Elkton, MD

Recall Details

Product Type
Devices
Report Date
April 12, 2023
Initiation Date
March 1, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
4940 units

Product Description

CAPIOX FX25 Hollow Fiber Oxygenator, Catalog Numbers 3CX*FX25REC, 3CX*FX25RWC

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 Pattern

US Nationwide. Belgium, Canada, Costa Rica, Thailand.

Code Information

UDI-DI: (01)00699753450868; Lot Number AM03