FDA recall Z-1575-2019

Maquet Cardiovascular, LLC · Class II · device

Product

Maquet Getinge-BEQ-T 46500 PRIME PACK Material:701065823

Reason for recall

Custom Tubing Sets for Extracorporeal Circulation (ECC)-During sterilization, the closed stopcock/non-vented cap configuration may prevent the flow of humidity/ethylene oxide gas into the fluid-path between the closed port and the non-vented cap therefore the Sterility Assurance Level (SAL) of the stopcock ports cannot be assured

Distribution

Nationwide

Key facts

Status
Terminated
Initiation date
2019-04-18
Report date
2019-06-05
Termination date
2025-07-28
Voluntary/Mandated
Voluntary: Firm initiated
Location
Wayne, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1575-2019