Medline recalls specific medical convenience kits due to potential out-of-specification endotoxin levels in Neurosponges. Affected kits include LAMINECTOMY PACK and ORTHO SPINE PACK models with listed SKUs and lot numbers.
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of endotoxin of the neurosponges.
Medline is recalling several medical convenience kits that contain Neurosponges with potential out-of-specification endotoxin levels. This could pose a risk to patients during medical procedures if the endotoxin levels are too high.
The Neurosponges in these kits may have endotoxin levels outside the specified safety range. Endotoxins are bacterial components that can cause infections or adverse reactions if they enter the body during medical procedures.
Healthcare professionals and patients using the recalled Medline medical convenience kits for procedures like laminectomy or spinal surgery. Those with the specific SKUs and lot numbers listed are most at risk.
Check for the product names: LAMINECTOMY PACK, ORTHO SPINE PACK, NEURO SPINE PACK, CRANIOTOMY PACK, SPINE PACK, or CRANI MT CARMEL. Look for the specific SKUs and lot numbers listed in the recall notice.
Identify the product name, SKU, and lot number to confirm if your kit is affected.
The Neurosponges in these kits may have endotoxin levels outside the specified safety range, which could pose a risk during medical procedures.
The affected kits include LAMINECTOMY PACK (SKU DYNJT6548), ORTHO SPINE PACK (SKU DYNJ44504G), NEURO SPINE PACK (SKU DYNJ45419F), and others with specific SKUs and lot numbers listed in the recall.
The recall does not require immediate stop use; however, affected kits should be checked and replaced if necessary.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2997-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2997-2026 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.
