Medline recalls 363 convenience kits with potential sterility issues due to calibration problems in sterilization equipment. Products include drawer sets, neuro carts, and suction trays with specific model numbers and lot numbers.
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 363 convenience kits that were sterilized using equipment with calibration issues. This could mean the products aren't sterile as intended, which is risky for medical use. The recall includes specific model numbers and lot numbers.
The sterilization equipment used to package these kits had calibration issues. This could mean the kits weren't properly sterilized, potentially leading to contamination if used on patients.
Healthcare facilities and medical professionals who use these convenience kits for patient care are most at risk. The recall affects products sold with specific model numbers and lot numbers listed in the notice.
Check for model numbers like ACC010326, ACC010326A, ACC010326B, ACC010475, ACC010542, ACC010543, and others listed in the recall. Also check the lot numbers provided in the notice.
Look for the model number and lot number on the product to confirm if it's in the recall list.
Reach out to Medline directly for assistance with the recall process.
The recall states there is a potential risk to sterility due to calibration issues, so they should not be used until the recall is resolved.
Check the model number and lot number on the product against the list provided in the recall notice.
Contact Medline directly for instructions on how to handle the recalled product.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2101-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2101-2026 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.
