Medline recalls convenience kits with potential contamination from improper sterilization. Affected kits may not be sterile, risking infection during medical procedures. 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 be contaminated during sterilization. This means the kits might not be sterile, increasing infection risk for medical procedures.
The sterilization process may not have been properly calibrated, leading to potential contamination. This could mean the kits are not sterile when used for medical procedures.
Healthcare workers using these kits for medical procedures are most at risk. The recall affects specific models sold in the U.S. during 2023.
Check for model number DYNDM1031A on the kit. Products were sold in the U.S. with lot numbers starting with 23EBM150.
Look for model number DYNDM103:1A on the kit label.
The recall states the kits may not be sterile due to sterilization issues, so they should not be used until the recall is addressed.
Check for model number DYNDM1031A and lot numbers starting with 23EBM150.
The recall does not specify a remedy, so contact Medline directly for instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1407-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1407-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.