Medline recalls convenience kits with potential sterility issues due to calibration problems in sterilization packaging. Affected models include ANCILLARY PACK-LF and OPEN HEART ANESTHESIA ICC-A kits.
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 process. This could lead to infections if the kits are used in medical procedures.
The calibration issues in the sterilization equipment could compromise the sterility assurance level of the kits. This means the kits might not be properly sterilized, increasing infection risk during medical procedures.
Healthcare professionals using these kits for medical procedures are most at risk. The recall affects specific models sold with certain lot numbers.
Check for model numbers DYNJ0185290G or DYNJ905567A. Lot numbers 21EBE777 through 24HBP446 are affected. These kits are sold by Medline Industries, LP.
Identify the model number and lot number on the kit to confirm if it's affected.
The recall indicates potential sterility issues, so they should not be used until confirmed safe by Medline.
Check for model numbers DYNJ0185290G or DYNJ905567A with lot numbers from 21EBE777 to 24HBP446.
The recall does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2089-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2089-2026 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.
