Reported May 6, 2026 · Ongoing

Medline medical procedure kits, containing Medline Neuro Sponges (4077 in total), LAMINECTOMY, CRANI, etc.

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 (4077 in total), LAMINECTOMY, CRANI, etc.
Lot codes and dates

284 of 284 products

Products covered by this recall
Model / numberBarcodesProduct as published
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 23CBR748
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 22LBP661
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 22JBI816
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 22JBI817
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 22GBG444
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 22GBG445
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 22FBM376
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 22DBB694
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 22DBA187
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 21LBP574
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 21JBU289
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 21FBS507
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 21FBL891
CDS780045N1019348935540640193489355407Medline Kit Number/ : UDI/DI each 10193489355406, UDI/DI case 40193489355407, Lot Number: 21BBF167
CDS780045O1019532736263840195327362639Medline Kit Number/ : UDI/DI each 10195327362638, UDI/DI case 40195327362639, Lot Number: 23FBU385
CDS780045O1019532736263840195327362639Medline Kit Number/ : UDI/DI each 10195327362638, UDI/DI case 40195327362639, Lot Number: 23EBT969
CDS780045O1019532736263840195327362639Medline Kit Number/ : UDI/DI each 10195327362638, UDI/DI case 40195327362639, Lot Number: 23DBP671
CDS780046O1088994276684040889942766841Medline Kit Number/ : UDI/DI each 10889942766840, UDI/DI case 40889942766841, Lot Number: 23BBA110
CDS780046O1088994276684040889942766841Medline Kit Number/ : UDI/DI each 10889942766840, UDI/DI case 40889942766841, Lot Number: 23ABK644
CDS780046O1088994276684040889942766841Medline Kit Number/ : UDI/DI each 10889942766840, UDI/DI case 40889942766841, Lot Number: 22KBH412
Amount recalled
1552486 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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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:57 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.