Medline recalls specific convenience kits due to potential calibration issues that could impact sterility assurance levels. Affected models include DYNJ56436A/B and others. 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 several convenience kits because calibration problems during sterilization might compromise their sterility. This means the kits could be contaminated, posing a risk of infection if used in medical settings.
The equipment used to sterilize and package these kits had calibration issues. This could lead to the kits not meeting the required sterility standards, potentially causing infections if used in medical procedures.
Healthcare professionals using these kits in medical settings are most at risk. Patients receiving treatments with the recalled kits could face infection risks if the kits are not properly sterile.
Check for model numbers DYNJ56436A, DYNJ56436B, DYNJRA1979, DYNJRA1979A, or SAMPA0108. Look for specific lot numbers listed in the recall notice.
Identify your kit's model number and lot number to confirm if it's affected by this recall.
Medline identified calibration issues during the sterilization process that could impact the sterility assurance level of the kits.
The recall notice does not specify a remedy; check the product details and contact Medline for further guidance.
The kits could be contaminated if not properly sterile, posing a risk of infection during medical procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1386-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1386-2026 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.
