Maquet recalls Getinge-BEQ-TOP 22701 tubing sets with batch numbers 3000060359, 3000060495, 3000062725, 3000071781 due to potential sterility issues during sterilization.
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 specific tubing sets for extracorporeal circulation (ECC) because their design may prevent proper sterilization. This could lead to infections if the tubing isn't properly sterilized.
The tubing's closed stopcock configuration 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 infections.
Healthcare professionals using these tubing sets for extracorporeal circulation procedures. Patients at risk during procedures using the recalled tubing sets.
Check for batch numbers: 3000060359, 3000060495, 3000062725, or 3000071781 on the tubing set. The product is labeled as Maquet Getinge-BEQ-TOP 22701 with material code 701050790.
Look for batch numbers 3000060359, 3000060495, 3000062725, or 3000071781 on the tubing set.
The tubing's closed stopcock configuration may prevent proper humidity and ethylene oxide gas flow during sterilization, risking infection.
Batch numbers 3000060359, 3000060495, 3000062725, and 3000071781.
Check for batch numbers 3000060359, 3000060495, 3000062725, or 3000071781 on the Maquet Getinge-BEQ-TOP 22701 tubing set with material code 701050790.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-1509-2019 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-1509-2019 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.
