Medline recalls convenience kits with model DYNJ50806L due to potential sterility risks from calibration problems during sterilization. Affected kits may not be sterile, risking infections.
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 convenience kits with model number DYNJ50806L because calibration issues during sterilization could compromise sterility. This means the kits might not be sterile, increasing infection risks for medical users.
The calibration issues in the sterilization equipment might lead to products not meeting sterility standards. This could allow contaminants to remain in the kits, potentially causing infections during medical procedures.
Healthcare workers using these kits for medical procedures are most at risk. Patients receiving treatments with non-sterile kits could face infection.
Check for model number DYNJ50806L on the kit. The kits were sold with lot numbers starting with 23FBK937 and UDI-DI numbers like 10195327344672.
Look for model number DYNJ50806L on the kit label.
Medline identified calibration issues in the sterilization equipment that could impact the sterility assurance level of the kits.
The kits may not be sterile, which could lead to infections during medical procedures.
Check for model number DYNJ50806L and lot numbers starting with 23FBK937.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1403-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1403-2026 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.
