Medline recalls 18 lots of ADMIT KIT (Model DYKA1343A) due to potential calibration issues that could impact sterility assurance. Consumers should check product details and contact Medline for guidance.
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 18 different lots of ADMIT KIT convenience kits because of calibration problems in the sterilization process. This could mean the kits aren't sterile as they should be, which is risky for medical use.
The sterilization equipment used to package these kits had calibration issues, which might lower the sterility assurance level. This means the kits could be contaminated, posing a risk of infection during medical procedures.
Healthcare professionals and medical facilities that use these kits for sterilizing medical devices are most at risk. The recall affects specific lots produced between 2021 and 2025.
Check for the model number DYKA1343A on the kit. The recall includes 18 specific lots with production dates from 2021 to 2025, labeled with lot numbers like 21CBV232 through 25LBC732.
Look for the model number DYKA1343A and lot numbers from 21CBV232 to 25LBC732 on the kit.
Medline identified calibration issues in the sterilization equipment that could impact the sterility assurance level of the kits.
Check for the model number DYKA1343A and lot numbers from 21CBV232 to 25LBC732 on the kit.
The recall does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2105-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2105-2026 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.
