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?

66 of 66 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ0532910L1019845950387040198459503871Medline Kit Number/ : UDI/DI each 10198459503870, UDI/DI case 40198459503871, Lot Number: 25IMD003
DYNJ0532910L1019845950387040198459503871Medline Kit Number/ : UDI/DI each 10198459503870, UDI/DI case 40198459503871, Lot Number: 25HMH643
DYNJ39461J1019532711272140195327112722Medline Kit Number/ : UDI/DI each 10195327112721, UDI/DI case 40195327112722, Lot Number: 22GBS127
DYNJ39461J1019532711272140195327112722Medline Kit Number/ : UDI/DI each 10195327112721, UDI/DI case 40195327112722, Lot Number: 22FBB472
DYNJ39461J1019532711272140195327112722Medline Kit Number/ : UDI/DI each 10195327112721, UDI/DI case 40195327112722, Lot Number: 25FBE752
DYNJ39461J1019532711272140195327112722Medline Kit Number/ : UDI/DI each 10195327112721, UDI/DI case 40195327112722, Lot Number: 25EBA260
DYNJ39461J1019532711272140195327112722Medline Kit Number/ : UDI/DI each 10195327112721, UDI/DI case 40195327112722, Lot Number: 25DBG176
DYNJ39461J1019532711272140195327112722Medline Kit Number/ : UDI/DI each 10195327112721, UDI/DI case 40195327112722, Lot Number: 25CBD819
DYNJ39461J1019532711272140195327112722Medline Kit Number/ : UDI/DI each 10195327112721, UDI/DI case 40195327112722, Lot Number: 25BBA593
DYNJ39461J1019532711272140195327112722Medline Kit Number/ : UDI/DI each 10195327112721, UDI/DI case 40195327112722, Lot Number: 24KBJ163
DYNJ58060I1019532732615940195327326150Medline Kit Number/ : UDI/DI each 10195327326159, UDI/DI case 40195327326150, Lot Number: 23KMI415
DYNJ58060I1019532732615940195327326150Medline Kit Number/ : UDI/DI each 10195327326159, UDI/DI case 40195327326150, Lot Number: 23JMK023
DYNJ58060I1019532732615940195327326150Medline Kit Number/ : UDI/DI each 10195327326159, UDI/DI case 40195327326150, Lot Number: 23JMB211
DYNJ58060I1019532732615940195327326150Medline Kit Number/ : UDI/DI each 10195327326159, UDI/DI case 40195327326150, Lot Number: 23IMC591
DYNJ58060I1019532732615940195327326150Medline Kit Number/ : UDI/DI each 10195327326159, UDI/DI case 40195327326150, Lot Number: 23HMG291
DYNJ58060I1019532732615940195327326150Medline Kit Number/ : UDI/DI each 10195327326159, UDI/DI case 40195327326150, Lot Number: 23GMG136
DYNJ58060I1019532732615940195327326150Medline Kit Number/ : UDI/DI each 10195327326159, UDI/DI case 40195327326150, Lot Number: 23FME285
DYNJ58060I1019532732615940195327326150Medline Kit Number/ : UDI/DI each 10195327326159, UDI/DI case 40195327326150, Lot Number: 23EME227
DYNJ58060I1019532732615940195327326150Medline Kit Number/ : UDI/DI each 10195327326159, UDI/DI case 40195327326150, Lot Number: 23CMD903
DYNJ58060I1019532732615940195327326150Medline Kit Number/ : UDI/DI each 10195327326159, UDI/DI case 40195327326150, Lot Number: 24KMI915
Amount recalled
9805 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, 6:57 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.