Medline recalls convenience kits for chest tube insertion, hernia repair, and breast/lung use due to potential sterility risks from calibration problems in sterilization packaging.
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
Medline is recalling several convenience kits used in medical procedures because calibration issues during sterilization could compromise their sterility. This means the products might not be safe for use, potentially leading to infections.
The calibration issues in the sterilization and packaging cycles might affect the sterility assurance level of the kits. This means the products could become contaminated during the process, increasing infection risk during medical procedures.
Healthcare professionals who use these kits for chest tube insertion, hernia repair, or breast/lung procedures are most at risk. Patients using these kits could face infection if the products are not sterile.
Check for model numbers DYNDA2941A, DYNJ83950, or DYNJ908337A/C with specific lot numbers listed in the recall notice. These kits were sold with certain serial numbers and production dates.
Review the model number and lot number on the kit to confirm if it's in the recall list.
Medline identified calibration issues in the sterilization and packaging cycles that could impact the sterility assurance level of the kits.
The recall states there is a potential risk to sterility, so the kits may not be safe for use and should be checked against the list.
Check the model number and lot number against the list provided in the recall notice to see if it's affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2106-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2106-2026 from Medline. 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.
