Medline recalls 1050 medical procedure kits containing Neuro Sponges with higher-than-expected endotoxin levels, which may be out of specification for endotoxin. Affected kits have specific UDI/DI and lot numbers listed in the recall.
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 1,050 medical procedure kits that contain Neuro Sponges with higher-than-expected endotoxin levels. This means the sponges may not meet the required endotoxin specifications, though the recall does not indicate a specific risk of injury.
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Neuro Sponge product. This indicates the product may be out of specification for endotoxin, but the recall does not describe a mechanism for injury or health effects.
Healthcare professionals and medical facilities that own or use these kits are most at risk. The recall does not specify any injuries or health effects.
Check for Medline kits with specific UDI/DI numbers and lot numbers listed in the recall. The affected kits include products with SKUs like CDS780056M, CDS980523L, and others with corresponding UDI/DI and lot numbers.
Review the UDI/DI and lot numbers on your Medline medical procedure kits to see if they match the affected items listed in the recall.
The recall states higher-than-expected endotoxin levels but does not describe any risk of injury or health effects.
Compare your kit's UDI/DI numbers and lot numbers with the specific numbers listed in the recall.
The recall does not specify a remedy or return process, so no action is required beyond checking if your kit is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2027-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2027-2026 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.
