FDA recall Z-0571-2025

LivaNova Deutschland GmbH · Class II · device

Product

Essenz HLM (Heart-Lung Machine), REF: 49-00-10, with Software

Reason for recall

Heart-Lung Machine GUI touchscreen may go dark for 10-15 seconds, safety/performance functions remain operational before reset, control maintained through backup control panel, but second reset may occur, may lead to gas blender standby, then gas blender must be reactivated using user interface on blender, sensors deactivated until new case started; GUI reset can lead to Hypoxia and Hypoperfusion.

Distribution

US Nationwide distribution in the states of CA, VA, GA, IN, NJ, FL, CO, MS, NV.

Key facts

Status
Ongoing
Initiation date
2024-10-18
Report date
2024-12-04
Voluntary/Mandated
Voluntary: Firm initiated
Location
Munich, Germany

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0571-2025