Maquet recalls specific Getinge-BEQ-T 8068 tubing sets due to potential sterility issues during sterilization. The closed stopcock design may prevent proper humidity and gas flow, risking contamination. Affected units have listed batch numbers.
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 certain Getinge-BEQ-T 8068 1/4" tubing sets with a bridge because their design might cause sterility problems during sterilization. This could lead to contaminated medical equipment if not properly sterilized.
During sterilization, the tubing's closed stopcock and non-vented cap configuration may block humidity and ethylene oxide gas from flowing into the fluid path. This could compromise the sterility assurance level, potentially leading to contaminated equipment.
Healthcare professionals using these tubing sets for extracorporeal circulation (ECC) systems are most at risk. The affected units have specific batch numbers listed in the recall notice.
Check for the model 'Getinge-BEQ-T 8068 1/4" With Bridge' and batch numbers: 3000041327, 3000042148, 3000042819, 3000046732, 3000054315, 3000055642, 3000062038, or 3000066689.
Identify the model number and batch numbers listed in the recall notice to confirm if your tubing set is affected.
The closed stopcock and non-vented cap design may prevent proper humidity and ethylene oxide gas flow during sterilization, risking contamination of medical equipment.
Batch numbers 3000041327, 3000042148, 3000042819, 3000046732, 3000054315, 3000055642, 3000062038, and 3000066689 are affected.
The recall record does not specify a remedy, so affected users should check with the manufacturer for guidance.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-1582-2019 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-1582-2019 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.
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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.
