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?

284 of 284 products

Products covered by this recall
Model / numberBarcodesProduct as published
CDS983493N1019845900021840198459000219Medline Kit Number/ : UDI/DI each 10198459000218, UDI/DI case 40198459000219, Lot Number: 25EDA675
CDS983493N1019845900021840198459000219Medline Kit Number/ : UDI/DI each 10198459000218, UDI/DI case 40198459000219, Lot Number: 25CDA718
CDS983493N1019845900021840198459000219Medline Kit Number/ : UDI/DI each 10198459000218, UDI/DI case 40198459000219, Lot Number: 25BDA328
CDS983493N1019845900021840198459000219Medline Kit Number/ : UDI/DI each 10198459000218, UDI/DI case 40198459000219, Lot Number: 24KDB408
CDS983493N1019845900021840198459000219Medline Kit Number/ : UDI/DI each 10198459000218, UDI/DI case 40198459000219, Lot Number: 24KDA607
DYNJ02476O1019532711947840195327119479Medline Kit Number/ : UDI/DI each 10195327119478, UDI/DI case 40195327119479, Lot Number: 23HMH658
DYNJ02476O1019532711947840195327119479Medline Kit Number/ : UDI/DI each 10195327119478, UDI/DI case 40195327119479, Lot Number: 23GMD341
DYNJ02476O1019532711947840195327119479Medline Kit Number/ : UDI/DI each 10195327119478, UDI/DI case 40195327119479, Lot Number: 23EMB793
DYNJ02476O1019532711947840195327119479Medline Kit Number/ : UDI/DI each 10195327119478, UDI/DI case 40195327119479, Lot Number: 23CMG372
DYNJ02476O1019532711947840195327119479Medline Kit Number/ : UDI/DI each 10195327119478, UDI/DI case 40195327119479, Lot Number: 23BMI499
DYNJ02476O1019532711947840195327119479Medline Kit Number/ : UDI/DI each 10195327119478, UDI/DI case 40195327119479, Lot Number: 22JMF967
DYNJ02476O1019532711947840195327119479Medline Kit Number/ : UDI/DI each 10195327119478, UDI/DI case 40195327119479, Lot Number: 22EMC648
DYNJ02476O1019532711947840195327119479Medline Kit Number/ : UDI/DI each 10195327119478, UDI/DI case 40195327119479, Lot Number: 22CMD889
DYNJ02476O1019532711947840195327119479Medline Kit Number/ : UDI/DI each 10195327119478, UDI/DI case 40195327119479, Lot Number: 24EMH897
DYNJ02476O1019532711947840195327119479Medline Kit Number/ : UDI/DI each 10195327119478, UDI/DI case 40195327119479, Lot Number: 24DMF264
DYNJ02476O1019532711947840195327119479Medline Kit Number/ : UDI/DI each 10195327119478, UDI/DI case 40195327119479, Lot Number: 24BMJ904
DYNJ02476O1019532711947840195327119479Medline Kit Number/ : UDI/DI each 10195327119478, UDI/DI case 40195327119479, Lot Number: 24AMH650
DYNJ0426069N1019532737131940195327371310Medline Kit Number/ : UDI/DI each 10195327371319, UDI/DI case 40195327371310, Lot Number: 23IME074
DYNJ0426069N1019532737131940195327371310Medline Kit Number/ : UDI/DI each 10195327371319, UDI/DI case 40195327371310, Lot Number: 23IMA416
DYNJ0426069N1019532737131940195327371310Medline Kit Number/ : UDI/DI each 10195327371319, UDI/DI case 40195327371310, Lot Number: 23EME302
Amount recalled
21288 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, 6:59 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.