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?

164 of 164 products

Products covered by this recall
Model / numberBarcodesProduct as published
CDS840402AI1019532733402440195327334025Medline Kit Number/ : UDI/DI each 10195327334024, UDI/DI case 40195327334025, Lot Number: 23JLA668
CDS840402AI1019532733402440195327334025Medline Kit Number/ : UDI/DI each 10195327334024, UDI/DI case 40195327334025, Lot Number: 23JLA240
CDS984890V1019845937436440198459374365Medline Kit Number/ : UDI/DI each 10198459374364, UDI/DI case 40198459374365, Lot Number: 25IMG470
CDS984890V1019845937436440198459374365Medline Kit Number/ : UDI/DI each 10198459374364, UDI/DI case 40198459374365, Lot Number: 25GMI158
CDS984890V1019845937436440198459374365Medline Kit Number/ : UDI/DI each 10198459374364, UDI/DI case 40198459374365, Lot Number: 25GMC404
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 23ILA647
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 23HLA953
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 23GLA064
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 23ELA715
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 22KLB111
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 22GLB222
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 22ELA384
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 22ELA314
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 22CLA246
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 22BLA951
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 22ALB037
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 21KLA949
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 21KLA323
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 21JLA776
DYNJ0394874L1019348980000540193489800006Medline Kit Number/ : UDI/DI each 10193489800005, UDI/DI case 40193489800006, Lot Number: 21ILA612
Amount recalled
4016 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.

Free recall alerts

Get alerted about new Medline Industries, LP recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:44 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.