Medline recalls specific neuro sponge packs due to higher-than-expected endotoxin levels, which may indicate the product is out of specification. Affected kits include Microdissection Packs with SKUs DYNJ80585B, DYNJ80585C, and DYNJ80585D.
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 certain medical procedure kits containing Neuro Sponges because internal testing found higher-than-expected endotoxin levels. This could mean the sponges don't meet safety standards for medical use, potentially causing infections or other complications during procedures.
Endotoxins are natural components of bacterial cell walls that can cause infections when introduced into the body. Higher-than-expected levels in these sponges may lead to adverse reactions during medical procedures, especially if the sponges are used in sterile environments.
Healthcare professionals using Medline Microdissection Packs with specific SKUs (DYNJ80585B, DYNJ80585C, DYNJ80585D) are most at risk. Patients undergoing surgery with these kits could face infection risks if the sponges are used without proper endotoxin testing.
Check for Microdissection Packs labeled with Medline, SKUs DYNJ80585B, DYNJ80585C, or DYNJ80585D. Each kit has a unique lot number (e.g., 22GBV101, 25EBT656) and UDI/DI codes (e.g., 10195327211158).
Look for Microdissection Packs with Medline labels and SKUs DYNJ80585B, DYNJ80585C, or DYNJ80585D.
Medline found higher-than-expected endotoxin levels in a representative neuro sponge product during internal testing, indicating the product may be out of specification for endotoxin levels.
The recall record does not specify a remedy, so no action is required beyond checking if your kits match the described SKUs and lot numbers.
The recall indicates a potential risk of infection due to higher endotoxin levels, but the record does not specify how likely this is in real-world use.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2030-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2030-2026 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.
