Medline recalls medical procedure kits with Neuro Sponges labeled SPNG NEURO 1X1 10/PK XR due to higher-than-expected endotoxin levels, potentially causing infections.
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 labeled SPNG NEURO 1X1 10/PK XR because these sponges may have higher-than-expected endotoxin levels. This could lead to infections if used in medical 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 increase the risk of infection during medical procedures.
Healthcare professionals using Medline Neuro Sponges in medical procedures may be affected. Patients undergoing procedures with these sponges could face infection risks.
Check for the label SPNG NEURO 1X1 10/PK XR on the kit. The kit number is DNSC38133, and lot numbers include 22KDA794, 22JDB440, and others listed in the recall.
Look for the label SPNG NEURO 1X1 10/PK XR on the medical procedure kit.
Medline identified higher-than-expected endotoxin levels in a representative Neuro Sponge product, indicating the in-market product may be out-of-specification for endotoxin.
Higher endotoxin levels could increase the risk of infection during medical procedures.
Check for the label SPNG NEURO 1X1 10/PK XR and the kit number DNSC38133 with specific lot numbers listed in the recall.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2032-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2032-2026 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.
