Medline recalls medical procedure kits with Neuro Sponges due to higher-than-expected endotoxin levels, which may indicate out-of-specification product. Check kit labels for listed SKUs and lot numbers to determine if affected.
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
Medline is recalling medical procedure kits containing Neuro Sponges because internal testing found higher-than-expected endotoxin levels in some products. This could mean the sponges don't meet quality standards for medical use.
Endotoxins are natural components in bacterial cell walls that can cause infections if introduced into the body. Higher-than-expected levels in the sponges may lead to contamination during medical procedures, though the risk is not immediate or severe.
Healthcare professionals and medical facilities using the recalled Medline Neuro Sponges in procedure kits are most at risk. The recall affects specific kits with listed SKUs and lot numbers.
Check the kit label for the product name and SKU (e.g., NEURO BASIN PACK-LF, SKU DYNJ0532910L). Look for the lot number and UDI/DI codes listed in the recall notice to confirm if your kit is affected.
Look for the product name and SKU on the kit label to determine if it matches the recalled items listed in the notice.
Medline identified higher-than-expected endotoxin levels in a representative Neuro Sponge product during internal testing, indicating some kits may be out-of-specification.
Check the kit label for the product name and SKU (e.g., NEURO BASIN PACK-LF, SKU DYNJ0532910L) and compare the lot number and UDI/DI codes to the list provided in the recall notice.
No action is needed if your kit does not match the listed SKUs and lot numbers in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2026-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2026-2026 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.
