Maquet recalls BEQ-TOP 38300 Adult CPS QID tubing sets due to potential sterility issues during sterilization. The closed stopcock design may prevent proper humidity and gas flow, risking contamination.
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
Maquet is recalling BEQ-TOP 38300 Adult CPS QID tubing sets because their design could cause sterility problems during sterilization. This means the tubing might not be safe for medical use after sterilization.
The tubing's closed stopcock and non-vented cap design may block humidity and ethylene oxide gas from flowing into the fluid path during sterilization. This could compromise the sterility assurance level, potentially leading to contamination.
Healthcare professionals using these tubing sets for extracorporeal circulation (ECC) procedures are most at risk. The affected units were sold with specific batch numbers.
Check for the model BEQ-TOP 38300 ADULT CPS QID with batch numbers 3000074735 or 3000080798. These units were sold by Maquet Getinge.
Identify the batch numbers 3000074735 or 3000080798 on the tubing set.
The closed stopcock design may prevent proper humidity and gas flow during sterilization, risking contamination.
The recall record does not specify a remedy, so contact Maquet Getinge directly for guidance.
Yes, batch numbers 3000074735 and 3000080798 are affected.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-1655-2019 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-1655-2019 from Maquet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
