Reported May 6, 2026 · Ongoing
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: SPINAL FUSION, Medline Kit…
Medline Industries, LP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
- Medline medical procedure kits, containing Medline Neuro Sponges
- labeled as followsSPINAL FUSION, Medline Kit Number/SKU CDS860017AG
- Lot codes and dates
- UDI/DI each 10198459237317
- UDI/DI case 40198459237318Lot
- Numbers
25LBI30825JBH22725HBQ37125HBP06925GBQ49425FBM67225CBF60325BBG22425ABN19025ABN214
- Amount recalled
- 120 kits
This recall covers 38 products
The agency filed one notice per product. You are reading one of them; the other 37 are below.
25 more are in the archive.
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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