FDA recall Z-1310-2024

Mc3 Inc · Class II · device

Product

NautilusTM Smart ECMO Module with Balance Biosurface-used in extracorporeal life support procedures to oxygenate blood, remove carbon dioxide and regulate blood temperature. Product Number: 48135, 48135E

Reason for recall

May have increased water path restriction within the heat exchanger, leading to degraded heat exchange performance during use. The reduction of water flow and reduced heat exchange performance may be experienced immediately upon priming or may worsen over the duration of use. The potential harm as stated in the IFU includes hypothermia due to inadequate heat transfer

Distribution

US Nationwide distribution.

Key facts

Status
Ongoing
Initiation date
2023-10-11
Report date
2024-03-27
Voluntary/Mandated
Voluntary: Firm initiated
Location
Dexter, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1310-2024