Medline recalls 52+ convenience kits for potential sterility issues due to calibration errors in sterilization packaging. All kits were exposed to validated cycles but may not meet sterility standards. Check model numbers and lot numbers listed to see if your kit is affected.
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 52 different convenience kits that were sterilized using equipment with calibration issues. This could mean the kits aren't sterile enough for medical use. If you have any of these kits, stop using them immediately.
The sterilization equipment used to package these kits had calibration issues. This means the kits might not be sterile after processing, increasing the risk of infection during medical procedures.
Healthcare professionals and medical facilities that use these kits for procedures. Patients receiving treatments with these kits are at risk of infection due to potential contamination.
Check if your kit has a model number listed in the recall (e.g., CDS860018G, DYKMBNDL138, DYNJ0305809O). Also look for the lot number (e.g., 21CBA213) and UDI-DI codes provided in the list.
Immediately stop using any recalled Medline convenience kits as they may not be sterile and could cause infections.
No, these kits have been recalled because the sterilization process may not have met sterility standards due to calibration issues.
Compare your kit's model number and lot number with the list provided in the recall notice.
Stop using it immediately and contact Medline for instructions on disposal or replacement.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2107-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2107-2026 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.
