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?

58 of 58 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ0751220P1019348981512240193489815123Medline Kit Number/ : UDI/DI each 10193489815122, UDI/DI case 40193489815123, Lot Number: 22EMB486
DYNJ0751220P1019348981512240193489815123Medline Kit Number/ : UDI/DI each 10193489815122, UDI/DI case 40193489815123, Lot Number: 22CMI117
DYNJ0751220P1019348981512240193489815123Medline Kit Number/ : UDI/DI each 10193489815122, UDI/DI case 40193489815123, Lot Number: 22CMB218
DYNJ0751220P1019348981512240193489815123Medline Kit Number/ : UDI/DI each 10193489815122, UDI/DI case 40193489815123, Lot Number: 22CMB219
DYNJ0751220P1019348981512240193489815123Medline Kit Number/ : UDI/DI each 10193489815122, UDI/DI case 40193489815123, Lot Number: 21LMA406
DYNJ0751220P1019348981512240193489815123Medline Kit Number/ : UDI/DI each 10193489815122, UDI/DI case 40193489815123, Lot Number: 21LMA805
DYNJ0751220P1019348981512240193489815123Medline Kit Number/ : UDI/DI each 10193489815122, UDI/DI case 40193489815123, Lot Number: 21JMF667
DYNJ0751220P1019348981512240193489815123Medline Kit Number/ : UDI/DI each 10193489815122, UDI/DI case 40193489815123, Lot Number: 21IMF752
DYNJ0751220P1019348981512240193489815123Medline Kit Number/ : UDI/DI each 10193489815122, UDI/DI case 40193489815123, Lot Number: 21HMG136
DYNJ0751220P1019348981512240193489815123Medline Kit Number/ : UDI/DI each 10193489815122, UDI/DI case 40193489815123, Lot Number: 21HMB278
DYNJ0751220P1019348981512240193489815123Medline Kit Number/ : UDI/DI each 10193489815122, UDI/DI case 40193489815123, Lot Number: 21GMD367
DYNJ0751220P1019348981512240193489815123Medline Kit Number/ : UDI/DI each 10193489815122, UDI/DI case 40193489815123, Lot Number: 21CKA503
DYNJ0751220P1019348981512240193489815123Medline Kit Number/ : UDI/DI each 10193489815122, UDI/DI case 40193489815123, Lot Number: 21AKA471
DYNJ47568B1019348984605840193489846059Medline Kit Number/ : UDI/DI each 10193489846058, UDI/DI case 40193489846059, Lot Number: 23JBT331
DYNJ47568B1019348984605840193489846059Medline Kit Number/ : UDI/DI each 10193489846058, UDI/DI case 40193489846059, Lot Number: 23IBL993
DYNJ47568B1019348984605840193489846059Medline Kit Number/ : UDI/DI each 10193489846058, UDI/DI case 40193489846059, Lot Number: 23GBN118
DYNJ47568B1019348984605840193489846059Medline Kit Number/ : UDI/DI each 10193489846058, UDI/DI case 40193489846059, Lot Number: 23FBQ324
DYNJ47568B1019348984605840193489846059Medline Kit Number/ : UDI/DI each 10193489846058, UDI/DI case 40193489846059, Lot Number: 23EBO916
DYNJ47568B1019348984605840193489846059Medline Kit Number/ : UDI/DI each 10193489846058, UDI/DI case 40193489846059, Lot Number: 23CBI861
DYNJ47568B1019348984605840193489846059Medline Kit Number/ : UDI/DI each 10193489846058, UDI/DI case 40193489846059, Lot Number: 23BBE825
Amount recalled
4324 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, 6:56 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.