Medline recalls three convenience kits due to potential contamination from sterilization calibration issues. Products may not be sterile, risking infections during medical procedures.
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 three types of convenience kits because their sterilization process might not have been properly calibrated, which could lead to contaminated products. This is serious because medical procedures require sterile equipment to prevent infections.
The sterilization equipment calibration issues mean the kits might not be sterile after packaging. This could lead to infections during medical procedures if the kits are used without proper sterility.
Healthcare workers using these kits for medical procedures are most at risk. Patients receiving procedures with contaminated kits could face infections.
Check for model numbers DYNJ15668R, DYNJ42829B, or DYNJT3437. Products were sold with specific lot numbers: 23HMB037, 22IBI084, or 25FBK633.
Look for model numbers DYNJ15668R, DYNJ42829B, or DYNJT3437 on the kit packaging.
Medline identified calibration issues in the sterilization equipment that could impact the sterility assurance level of the kits.
Patients using contaminated kits during medical procedures could face infection risks, but the recall is for healthcare workers to ensure safety.
Check for model numbers DYNJ15668R, DYNJ42829B, or DYNJT3437 with lot numbers 23HMB037, 22IBI084, or 25FBK633.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1404-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1404-2026 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.
