Medline recalls medical procedure kits with Neuro Sponges labeled for bronchoscopy 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 that include Neuro Sponges labeled for bronchoscopy because these sponges may have higher-than-expected endotoxin levels. This could mean the sponges don't meet safety standards and might pose a risk to patients during medical procedures.
Endotoxins are natural components of bacterial cell walls that can cause inflammation or infection if introduced into the body. Higher-than-expected levels in these sponges could lead to adverse reactions during medical procedures, though the risk is not severe.
Healthcare professionals using Medline Neuro Sponges labeled for bronchoscopy are likely affected. Patients undergoing procedures with these sponges may be at slightly higher risk due to potential endotoxin levels.
Check for Medline kits labeled 'EH BRONCHOSCOPY' with SKU DYNJT3270. Look for lot numbers 26AMF231, 25GMC304, or 25DMF469 on the packaging.
Look for the label 'EH BRONCHOSCOPY' and SKU DYNJT3270 on the kit packaging.
Medline identified higher-than-expected endotoxin levels in some Neuro Sponges during an internal review, indicating the product may not meet safety standards.
The recall record does not specify a remedy, so no action is required beyond checking if your product matches the described details.
The recall indicates potential higher endotoxin levels, which could cause inflammation or infection during medical procedures, but the risk is not severe.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2010-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2010-2026 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.
