Medela recalls AXS Universal Aspiration Tubing with incorrect expiration date label. Correct date should be 2021-07-24, not 2023-07-24. This may lead to using expired sterile tubing.
Incorrect expiration date of "2023-07-24" on label of sterile tubing. Correct expiration date should be "2021-07-24".
Medela is recalling AXS Universal Aspiration Tubing due to an incorrect expiration date on the label. Using this tubing could lead to using expired sterile products, which might not be safe for medical procedures.
The tubing has an incorrect expiration date label showing 2023-07-24 instead of the correct 2021-07-24. Using expired sterile tubing could lead to potential safety issues during medical procedures.
Healthcare professionals using Medela AXS Universal Aspiration Tubing with the Dominant Flex Surgical Suction Pump are likely affected. Those using the tubing for medical procedures are at higher risk.
Check for the product name 'AXS Universal Aspiration Tubing' with the serial number 07612367053921. The tubing is used with the Dominant Flex Surgical Suction Pump.
Verify the expiration date on the tubing label. The correct date should be 2021-07-24, not 2023-07-24.
The tubing has an incorrect expiration date label showing 2023-07-24 instead of the correct 2021-07-24.
The recall record does not mention a remedy or fix for this issue.
Check for the product name 'AXS Universal Aspiration Tubing' with the serial number 07612367053921. The tubing is used with the Dominant Flex Surgical Suction Pump.
We’ve drafted a message you can send Medela to request your refund or repair — edit it as you like.
Subject: Recall Z-1502-2021 — Medela Medela Hello, I own a Medela that is covered by recall Z-1502-2021 from Medela. 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.