Maquet Cardiovascular, LLC recalls Maquet Getinge-BEQ-TOP 50903 Custom ECC Pk-Pdtrc 3/8 - Material: 709000078R01

Recall date

April 18, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1675-2019

FDA classification

Class II

Brand / firm

Maquet Cardiovascular, LLC

Sold / distributed

Nationwide

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Maquet Getinge-BEQ-TOP 50903 Custom ECC Pk-Pdtrc 3/8 - Material: 709000078R01