Medline recalls convenience kits with potential sterility issues due to calibration problems during sterilization. Affected kits may not be sterile, risking infections. Contact Medline for details.
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 could have sterility issues because of calibration problems during sterilization. This means the kits might not be sterile, increasing infection risk.
The calibration issues during sterilization could lead to the kits not being properly sterile. This means the kits might not meet the required sterility standards, potentially causing infections.
Healthcare workers using these kits for medical procedures are most at risk. Patients receiving care with these kits could face infection risks.
Check for model number DYNDM1031A on the kit. The lot number 23EBM150 and serial numbers 10884389555897 (each) and 40884389555898 (case) are also on the kits.
Look for model number DYNDM1031A on the kit.
Reach out to Medline for specific instructions on next steps.
Medline identified calibration issues during sterilization that could impact the sterility assurance level of the kits.
Check for model number DYNDM1031A, lot number 23EBM150, and serial numbers 10884389555897 (each) or 40884389555898 (case).
Contact Medline for specific instructions on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2123-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2123-2026 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.
