The Recall Desk

FDA (Devices) recall action 82703

Maquet Cardiovascular, LLC recalled 183 products on 2019-06-05

The FDA (Devices) publishes a recall like this one as 183 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 183 pages.

Products
183
Announced
2019-06-05
Critical
0
Units

Why these products were 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

The agency’s own wording, quoted from the enforcement report.

51–75 of 183