FDAFDA · Food and drugs·Recall number Z-1518-2019
Maquet Getinge-BEQ-TOP 1601#QUADROX iD - Pack Material:701052285
Published June 5, 2019 · Recall initiated: April 18, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Maquet Cardiovascular, LLC
- Distributor
- Nationwide
- Lot
- Batch Numbers: 3000048235 3000056129 3000059730 3000065496 3000070700 3000073428
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.