Medline recalls convenience kits with potential sterility issues due to calibration problems in sterilization equipment. Affected models include DYNJ83950 with specific lot numbers.
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 that may not be sterile because of calibration issues in the sterilization equipment used to make them. This could lead to infections if the kits are used for medical purposes.
The sterilization equipment used to package the kits had calibration issues, which might compromise the sterility of the products. This means the kits could become contaminated during the packaging process.
Healthcare workers using these kits for medical procedures are most at risk. Patients receiving treatments with these kits could face infection risks.
Check for model number DYNJ83950 and lot numbers 24DBT832, 24CBH626, 23LBR075, 23FBF248, or 23CBG610 on the packaging or label.
Look for model number DYNJ83950 and specific lot numbers listed in the recall notice.
Medline identified calibration issues in the sterilization equipment that could impact the sterility assurance level of the kits.
The recall notice does not specify a remedy, so check the product details and contact Medline for further instructions.
The kits may not be sterile, which could lead to infections if used for 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-1412-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1412-2026 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.
