medical Class II Updated 2018-06-20

Datascope Corporation recalls Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 4906 P

Recalled Product

Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 4906 PEDIARIC CPB PACK, Part Number 701056041 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.


Hazard / Issue

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

Issued by

FDA

Affected States: IA, FL
Lot/Code Info: UDI 0607567203600
View official government recall

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