FDA recall Z-1831-2024

Maquet Medical Systems USA · Class II · device

Product

CARDIOHELP-i System. Blood oxygenation and carbon dioxide removal system.

Reason for recall

The firm identified that the measured patient leakage current in some devices significantly exceeded expected levels.

Distribution

US Nationwide distribution in the states of NJ & TX.

Key facts

Status
Ongoing
Initiation date
2024-04-15
Report date
2024-05-22
Voluntary/Mandated
Voluntary: Firm initiated
Location
Wayne, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1831-2024