FDA recall Z-1652-2019

Product

Maquet Getinge- BEQ-TOP 37200 E-Circuit Bioline Heparin Material: 701055388R01

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-1652-2019