Reported May 6, 2026 · Ongoing

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows

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?

18 of 18 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ904269B1019348925163040193489251631Medline Kit Number/ : UDI/DI each 10193489251630, UDI/DI case 40193489251631, Lot Number: 21KBM212
DYNJ904269B1019348925163040193489251631Medline Kit Number/ : UDI/DI each 10193489251630, UDI/DI case 40193489251631, Lot Number: 21IBT678
DYNJ904269B1019348925163040193489251631Medline Kit Number/ : UDI/DI each 10193489251630, UDI/DI case 40193489251631, Lot Number: 21GBF973
DYNJ904269B1019348925163040193489251631Medline Kit Number/ : UDI/DI each 10193489251630, UDI/DI case 40193489251631, Lot Number: 21EBR775
DYNJ904269B1019348925163040193489251631Medline Kit Number/ : UDI/DI each 10193489251630, UDI/DI case 40193489251631, Lot Number: 21DBH715
DYNJ904269B1019348925163040193489251631Medline Kit Number/ : UDI/DI each 10193489251630, UDI/DI case 40193489251631, Lot Number: 21BBI962
DYNJ904269C1019532704007940195327040070Medline Kit Number/ : UDI/DI each 10195327040079, UDI/DI case 40195327040070, Lot Number: 22HBO534
DYNJ904269C1019532704007940195327040070Medline Kit Number/ : UDI/DI each 10195327040079, UDI/DI case 40195327040070, Lot Number: 22FBY086
DYNJ904269C1019532704007940195327040070Medline Kit Number/ : UDI/DI each 10195327040079, UDI/DI case 40195327040070, Lot Number: 22FBG752
DYNJ904269C1019532704007940195327040070Medline Kit Number/ : UDI/DI each 10195327040079, UDI/DI case 40195327040070, Lot Number: 22CBY116
DYNJ904269C1019532704007940195327040070Medline Kit Number/ : UDI/DI each 10195327040079, UDI/DI case 40195327040070, Lot Number: 22ABS155
DYNJ904269C1019532704007940195327040070Medline Kit Number/ : UDI/DI each 10195327040079, UDI/DI case 40195327040070, Lot Number: 21LBF114
DYNJ904269D1019532727593840195327275939Medline Kit Number/ : UDI/DI each 10195327275938, UDI/DI case 40195327275939, Lot Number: 23JBN926
DYNJ904269D1019532727593840195327275939Medline Kit Number/ : UDI/DI each 10195327275938, UDI/DI case 40195327275939, Lot Number: 23FBE547
DYNJ904269D1019532727593840195327275939Medline Kit Number/ : UDI/DI each 10195327275938, UDI/DI case 40195327275939, Lot Number: 23EBI633
DYNJ904269D1019532727593840195327275939Medline Kit Number/ : UDI/DI each 10195327275938, UDI/DI case 40195327275939, Lot Number: 23DBA946
DYNJ904269D1019532727593840195327275939Medline Kit Number/ : UDI/DI each 10195327275938, UDI/DI case 40195327275939, Lot Number: 23CBD209
DYNJ904269D1019532727593840195327275939Medline Kit Number/ : UDI/DI each 10195327275938, UDI/DI case 40195327275939, Lot Number: 23ABH377.
Amount recalled
632 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, 7:35 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.