Medline recalls convenience kits with model DYNJ50806L due to potential sterility risks from calibration errors during sterilization. Affected kits may not be sterile, risking infection.
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 risk for medical users.
The calibration issues during sterilization could lead to the kits not being properly sterile. This means medical procedures might be performed with non-sterile equipment, potentially causing infections.
Healthcare workers using these kits for medical procedures are most at risk. The recall affects kits sold with specific model numbers and lot numbers.
Check for model number DYNJ50806L on the kit. The lot numbers 23FBK937 and UDI-DI numbers 10195327344672 (each) and 40195327344673 (case) are also indicators of affected units.
Verify the model number and lot numbers to confirm if your kit is affected.
Medline identified calibration issues during sterilization that could impact the sterility assurance level of the kits.
Look for model number DYNJ50806L, lot number 23FBK937, or UDI-DI numbers 10195327344672 (each) and 40195327344673 (case).
The recall does not specify a remedy, so check with Medline for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2119-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2119-2026 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.
