FDA recall Z-0550-2022

Abiomed, Inc. · Class I · device

Product

OXY-1 System, Model Number 001-0500-001. Used during cardiopulmonary bypass. OXY-1 System consists of Console, Pump Drive, E Drive, and Pole Mount. The disposable Pump Lung Unit PLU part number 001-0400-100 is sold separately and is not part of this recall.

Reason for recall

The firm has received complaints of the OXY-1 System Console experiencing a power interruption while in use, which disrupts therapy delivered to a patient on support. Disruption of therapy could lead to prolonged hypoxia.

Distribution

US distribution to FL, GA, IN, MD, NC, PA, TX.

Key facts

Status
Terminated
Initiation date
2021-12-14
Report date
2022-02-09
Termination date
2023-02-28
Voluntary/Mandated
Voluntary: Firm initiated
Location
Danvers, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0550-2022