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?

40 of 40 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ0578916X1019348928838440193489288385Medline Kit Number/ : UDI/DI each 10193489288384, UDI/DI case 40193489288385, Lot Number: 23IME618
DYNJ0578916X1019348928838440193489288385Medline Kit Number/ : UDI/DI each 10193489288384, UDI/DI case 40193489288385, Lot Number: 23FMF542
DYNJ0578916X1019348928838440193489288385Medline Kit Number/ : UDI/DI each 10193489288384, UDI/DI case 40193489288385, Lot Number: 23DMA094
DYNJ0578916X1019348928838440193489288385Medline Kit Number/ : UDI/DI each 10193489288384, UDI/DI case 40193489288385, Lot Number: 23AMD730
DYNJ0578916X1019348928838440193489288385Medline Kit Number/ : UDI/DI each 10193489288384, UDI/DI case 40193489288385, Lot Number: 22GMB685
DYNJ0578916X1019348928838440193489288385Medline Kit Number/ : UDI/DI each 10193489288384, UDI/DI case 40193489288385, Lot Number: 22DMI233
DYNJ0578916X1019348928838440193489288385Medline Kit Number/ : UDI/DI each 10193489288384, UDI/DI case 40193489288385, Lot Number: 22DMC612
DYNJ0578916X1019348928838440193489288385Medline Kit Number/ : UDI/DI each 10193489288384, UDI/DI case 40193489288385, Lot Number: 24AMA230
DYNJ51637D1019532763210640195327632107Medline Kit Number/ : UDI/DI each 10195327632106, UDI/DI case 40195327632107, Lot Number: 24GMI248
DYNJ656501019348928564240193489285643Medline Kit Number/ : UDI/DI each 10193489285642, UDI/DI case 40193489285643, Lot Number: 23JMK002
DYNJ656501019348928564240193489285643Medline Kit Number/ : UDI/DI each 10193489285642, UDI/DI case 40193489285643, Lot Number: 23JME739
DYNJ656501019348928564240193489285643Medline Kit Number/ : UDI/DI each 10193489285642, UDI/DI case 40193489285643, Lot Number: 23IBJ883
DYNJ656501019348928564240193489285643Medline Kit Number/ : UDI/DI each 10193489285642, UDI/DI case 40193489285643, Lot Number: 23EBO648
DYNJ656501019348928564240193489285643Medline Kit Number/ : UDI/DI each 10193489285642, UDI/DI case 40193489285643, Lot Number: 23ABT378
DYNJ656501019348928564240193489285643Medline Kit Number/ : UDI/DI each 10193489285642, UDI/DI case 40193489285643, Lot Number: 22KBG029
DYNJ656501019348928564240193489285643Medline Kit Number/ : UDI/DI each 10193489285642, UDI/DI case 40193489285643, Lot Number: 22JBF057
DYNJ656501019348928564240193489285643Medline Kit Number/ : UDI/DI each 10193489285642, UDI/DI case 40193489285643, Lot Number: 22IBL935
DYNJ656501019348928564240193489285643Medline Kit Number/ : UDI/DI each 10193489285642, UDI/DI case 40193489285643, Lot Number: 22FBD348
DYNJ656501019348928564240193489285643Medline Kit Number/ : UDI/DI each 10193489285642, UDI/DI case 40193489285643, Lot Number: 22DBP280
DYNJ656501019348928564240193489285643Medline Kit Number/ : UDI/DI each 10193489285642, UDI/DI case 40193489285643, Lot Number: 22BBB689
Amount recalled
3170 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.

Want the full recall guide?

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, 6:16 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.