Medline recalls specific convenience kits for urology use due to potential sterility issues from calibration problems in sterilization packaging. Affected kits include models DYKMBNDL106, DYKMBNDL106A, DYKMBNDL188, DYKMBNDL189, and DYKMBNDL189A with specific lot numbers.
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 urology convenience kits because calibration issues in their sterilization process could compromise the sterility of the products. This means the kits might not be clean enough for medical use, posing a risk of infection to patients.
The calibration issues in the sterilization equipment could lead to products not meeting the required sterility standards. This means the kits might be contaminated, increasing the risk of infection during medical procedures.
Healthcare professionals using these kits for urological procedures are most at risk. Patients receiving treatments with these kits could face infection if the products are not sterile.
Check for model numbers DYKMBNDL106, DYKMBNDL106A, DYKMBNDL188, DYKMBNDL189, or DYKMBNDL189A. Look for specific lot numbers listed in the recall notice, such as 21ABJ542, 21BBG085, and others.
Identify the model number on the kit to see if it matches the recalled models: DYKMBNDL106, DYKMBNDL106A, DYKMBNDL188, DYKMBNDL189, or DYKMBNDL189A.
Reach out to Medline Industries for assistance with the recall, including instructions on how to return or replace the affected kits.
The recall indicates potential sterility issues, so they should not be used until the recall is resolved. Medline has identified calibration problems that could compromise sterility.
Contact Medline Industries directly to determine if your kit is affected and to get instructions for returning or replacing it.
Check the model number and lot number on the kit. Affected kits have specific model numbers and lot numbers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2126-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2126-2026 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.
