Medline recalls medical procedure kits with Neuro Sponges due to higher-than-expected endotoxin levels. Affected kits may not meet safety standards. Consumers should check labels for specific model 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 because tests found higher-than-expected endotoxin levels. This could mean the products don't meet safety standards and might pose a risk to users.
Endotoxins are natural components of bacterial cell walls that can cause infections or allergic reactions when introduced into the body. Higher-than-expected levels in these sponges may increase the risk of adverse health effects during medical procedures.
Healthcare professionals and medical facilities using the recalled Medline procedure kits are most at risk. The recall affects specific model numbers and lot numbers listed in the notice.
Check for the label 'GENERAL KIT, Medline Kit' on the product. The specific model numbers include DYNJ905664I, and lot numbers 24KME456 and 24HMJ900.
Look for the label 'GENERAL KIT, Medline Kit' and the model number DYNJ905664I.
The recall states higher-than-expected endotoxin levels, which could mean the sponges don't meet safety standards for medical use.
Check for the label 'GENERAL KIT, Medline Kit' and model number DYNJ905664I, with lot numbers 24KME456 or 24HMJ900.
The recall does not specify a stop-use instruction, so users can continue using the kits but should check if they are affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2031-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2031-2026 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.
