FDA recall Z-2180-2018

Datascope Corporation · Class II · device

Product

Maquet Cardiopulmonary Bypass Custom Tubing kit BO-TOP 38600 ADULT CPB, Part Number 701056035R01 Product Usage: The Maquet Cardiopulmonary Bypass Custom Tubing kit is a sterile, non-pyrogenic device for single use only and is not to be re-sterilized by the user. The product consists of tubing and connectors with connected oxygenators, reservoirs, filters and other cardiopulmonary bypass components assembled into user specified circuits for procedures requiring extracorporeal support for up to six hours. See Attachment 6 for a copy of MCP Instructions for Use.

Reason for recall

There is a potential for the over-pressure safety (OPS) valve in the tubing kits to not allow flow through.

Distribution

The products were distributed to the following US states: IA and FL.

Key facts

Status
Terminated
Initiation date
2017-07-27
Report date
2018-06-20
Termination date
2020-02-07
Voluntary/Mandated
Voluntary: Firm initiated
Location
Fairfield, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2180-2018