Medline recalls Centurion EP Lab Instrument Kit (MNS10480) with lot 23LBK889 due to potential non-sterile product if pouch seal is opened. Affected users should check their kit's lot number and contact Medline for details.
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
Medline is recalling Centurion EP Lab Instrument Kits with lot number 23LBK889 because opening the breather pouch seal could lead to using non-sterile products. This poses a risk for medical procedures where sterile conditions are critical.
The breather pouch seal on the kit may open or become unsealed, allowing non-sterile product to be used during medical procedures. This could compromise infection control and patient safety if the pouch is opened.
Medical professionals and healthcare facilities using the Centurion EP Lab Instrument Kit with lot number 23LBK889 are most at risk. The recall affects kits sold in the U.S. with specific lot numbers.
Check the lot number on the kit's packaging, which is 23LBK889 for this recall. The product is a Centurion EP Lab Instrument Kit with reference number MNS10480.
Look for the lot number 23LBK889 on the packaging to confirm if your kit is affected.
The affected lot number is 23LBK889.
The recall is due to the potential for non-sterile product use if the breather pouch seal is opened or unsealed.
Check the lot number on the packaging; if it is 23LBK889, your kit is affected.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0149-2025 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0149-2025 from Medline Industries. 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.
