Reported May 6, 2026 · Ongoing

Medline medical procedure kits, containing Medline Neuro Sponges (102 in total)

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 (102 in total)
Lot codes and dates

283 of 283 products

Products covered by this recall
Model / numberBarcodesProduct as published
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 23KBN711
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 23GBD593
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 23GBD781
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 23DBF906
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 22LBI985
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 22KBC504
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 22IBF741
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 22FBX069
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 22DBS948
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 22CBX667
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 21IBT137
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 21HBG608
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 25GBV215
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 25GBA852
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 24KBJ988
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 24JBC528
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 24IBV131
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 24IBP386
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 24GBA976
CDS980375L1019348992288240193489922883Medline Kit Number/ : UDI/DI each 10193489922882, UDI/DI case 40193489922883, Lot Number: 24CBU492
Amount recalled
22116 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:40 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.