Medline recalls medical procedure kits with Neuro Sponges that may have higher-than-expected endotoxin levels. Affected kits include specific SKUs and lot numbers. Consumers should check their kits for the listed identifiers.
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 that were found to have higher-than-expected endotoxin levels during internal testing. This could mean the products are out of specification and may pose a risk if used in medical procedures.
Endotoxins are natural components of bacterial cell walls that can cause infections or immune reactions when introduced into the body. Higher-than-expected levels in these sponges could lead to adverse reactions during medical procedures if the products are used improperly.
Healthcare professionals and medical facilities that own or use the recalled Medline Neuro Sponges kits. The risk is primarily for those using the products in clinical settings where endotoxin levels could affect patient safety.
Check for Medline kits labeled 'ENDOSCOPIC SKULL BASE' or 'ENT ENDO SINUS WILMINGTON PACK' with specific SKUs: DYNJ58648J, DYNJ66447, or DYNJ908362B. Look for lot numbers matching the listed sequences (e.g., 23JMD938, 23HMG766, etc.).
Look for the specific Medline kit labels and lot numbers listed in the recall notice to confirm if your product is affected.
Medline identified higher-than-expected endotoxin levels in a representative sample of their Neuro Sponges during an internal review, indicating the products may be out of specification.
Check your Medline kits for the specific SKUs and lot numbers listed in the recall notice to determine if they are affected. No action is required if your product does not match the identifiers.
The recall indicates potential endotoxin levels above specifications, which could cause infections or immune reactions during medical procedures. However, the risk is low for typical use and not immediate.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2023-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2023-2026 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.
