Medline recalls medical procedure kits containing Neuro Sponges labeled ENDOSCOPY-LF due to higher-than-expected endotoxin levels in some units. Affected kits include specific SKUs and lot numbers.
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 that contain Neuro Sponges labeled ENDOSCOPY-LF because internal testing found higher-than-expected endotoxin levels in some units. This could mean the products are out of specification for endotoxin, though the recall does not specify a risk of injury.
Endotoxins are natural components of bacterial cell walls that can cause inflammation or infection if introduced into the body. The recall indicates that some Medline Neuro Sponges had higher-than-expected endotoxin levels, which could potentially lead to an increased risk of infection or adverse reactions during medical procedures.
Healthcare professionals and medical facilities using Medline's ENDOSCOPY-LF labeled procedure kits with Neuro Sponges are likely affected. The risk is minimal as the issue relates to endotoxin levels, which are typically not a direct health hazard in normal use.
Check for Medline procedure kits labeled ENDOSCOPY-LF with specific SKUs: DYNJ22890M, DYNJ40645B, DYNJ42319C, DYNJ66449, DYNJ900282I, DYNJ902831D, or DYNJ906630. Look for lot numbers listed in the recall details.
Identify if your kit has the listed SKUs and lot numbers from the recall notice.
Medline identified higher-than-expected endotoxin levels in some Neuro Sponges during internal testing, indicating the products may be out of specification for endotoxin.
The recall does not specify a risk of injury, so there is no immediate need to stop using the kits. However, you should check if your kit matches the listed SKUs and lot numbers.
The recall does not provide a specific remedy, so you should check the product details to see if your kit is affected and contact Medline for further guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2024-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2024-2026 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.
