RecallRadar

FDA Device recall Z-1310-2024

NautilusTM Smart ECMO Module with Balance Biosurface-used in extracorporeal life support procedures to oxygenate blood, remove carbon dioxi…

On 2024-03-27 the FDA classified a Class II recall of NautilusTM Smart ECMO Module with Balance Biosurface-used in extracorporeal life support procedures to oxygenate blood, remove carbon dioxi… by Mc3, citing 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 exchang….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1310-2024
ClassificationClass II
Statusongoing
Initiated2023-10-11
Published2024-03-27
Last updated2026-09-13 11:57 UTC
CompanyMc3
DistributionUS

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

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

Identifiers

code_infoGTIN:(1)10854916006871; (2)10854916006895 All Serial Numbers between 481022923 and 481024039

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1310-2024%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.