Medline recalls medical procedure kits with Neuro Sponges labeled ANGIO PACK-LF due to higher-than-expected endotoxin levels, potentially affecting product safety.
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 labeled 'ANGIO PACK-LF' because they may have higher-than-expected endotoxin levels. This could pose a risk to patient safety during medical procedures.
Endotoxins are natural components of bacterial cell walls that can cause infections or adverse reactions when introduced into the body. Higher-than-expected levels in these sponges may increase the risk of infection or complications during medical procedures.
Healthcare professionals using Medline medical procedure kits with Neuro Sponges labeled 'ANGIO PACK-LF' are likely affected. Patients receiving procedures using these kits may be at risk.
Check for kits labeled 'ANGIO PACK-LF' with Medline Neuro Sponges. The kit number is DYNJ0774765U, and the lot number is 24ILA931.
Look for the label 'ANGIO PACK-LF' on the medical procedure kit containing Medline Neuro Sponges.
Medline identified higher-than-expected endotoxin levels in a representative Neuro Sponge product during an internal review, indicating the product may be out-of-specification for endotoxin.
The recall record does not specify a remedy, so no action is required beyond checking if you have the labeled product.
The recall indicates potential higher endotoxin levels, which could pose a risk during medical procedures, but the record does not specify if the product is unsafe in normal use.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2014-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2014-2026 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.
