Medline recalls two convenience kit models due to potential sterility risks from calibration issues during sterilization. Affected products may not meet sterility standards.
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 two specific convenience kits because their sterilization process might not be working properly, which could mean the kits aren't sterile enough. This is important for healthcare workers who use these kits for medical procedures.
The equipment used to sterilize these kits might not be calibrated correctly, which could lead to the kits not being sterile enough. This means the kits might not meet the required sterility standards for medical use.
Healthcare workers using Medline Convenience Kits for medical procedures are most at risk. The recall affects specific models sold with certain lot numbers.
Check for model numbers DYNJ353:363A (DRAPE PACK) or SPTPCD10005 (SICK KIDS-GENERAL CUSTOM SPLIT). Products with lot numbers 21BBP020 or 24JBB041 are affected.
Look for model numbers DYNJ35363A or SPTPCD10005 and lot numbers 21BBP020 or 24JBB041 on the product.
The recall states that the kits may not meet sterility standards due to calibration issues, so they should not be used until the recall is addressed.
Check for model numbers DYNJ35363A (DRAPE PACK) or SPTPCD10005 (SICK KIDS-GENERAL CUSTOM SPLIT) with lot numbers 21BBP020 or 24JBB041.
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-2124-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2124-2026 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.
