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?

52 of 52 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ0045920D1019532726740740195327267408Medline Kit Number/ : UDI/DI each 10195327267407, UDI/DI case 40195327267408, Lot Number: 23JMB165
DYNJ0045920D1019532726740740195327267408Medline Kit Number/ : UDI/DI each 10195327267407, UDI/DI case 40195327267408, Lot Number: 23CMH103
DYNJ0045920D1019532726740740195327267408Medline Kit Number/ : UDI/DI each 10195327267407, UDI/DI case 40195327267408, Lot Number: 23BMH200
DYNJ0045920D1019532726740740195327267408Medline Kit Number/ : UDI/DI each 10195327267407, UDI/DI case 40195327267408, Lot Number: 23BMB495
DYNJ0045920D1019532726740740195327267408Medline Kit Number/ : UDI/DI each 10195327267407, UDI/DI case 40195327267408, Lot Number: 22KMH108
DYNJ0045920D1019532726740740195327267408Medline Kit Number/ : UDI/DI each 10195327267407, UDI/DI case 40195327267408, Lot Number: 22KME285
DYNJ0045920D1019532726740740195327267408Medline Kit Number/ : UDI/DI each 10195327267407, UDI/DI case 40195327267408, Lot Number: 23KMJ648
DYNJ0045920F1019532764371340195327643714Medline Kit Number/ : UDI/DI each 10195327643713, UDI/DI case 40195327643714, Lot Number: 26BME013
DYNJ0045920F1019532764371340195327643714Medline Kit Number/ : UDI/DI each 10195327643713, UDI/DI case 40195327643714, Lot Number: 25JMC725
DYNJ0045920F1019532764371340195327643714Medline Kit Number/ : UDI/DI each 10195327643713, UDI/DI case 40195327643714, Lot Number: 25IMA571
DYNJ0045920F1019532764371340195327643714Medline Kit Number/ : UDI/DI each 10195327643713, UDI/DI case 40195327643714, Lot Number: 25HMC497
DYNJ0045920F1019532764371340195327643714Medline Kit Number/ : UDI/DI each 10195327643713, UDI/DI case 40195327643714, Lot Number: 25FMG199
DYNJ0045920F1019532764371340195327643714Medline Kit Number/ : UDI/DI each 10195327643713, UDI/DI case 40195327643714, Lot Number: 25EMB523
DYNJ0045920F1019532764371340195327643714Medline Kit Number/ : UDI/DI each 10195327643713, UDI/DI case 40195327643714, Lot Number: 25DMF918
DYNJ0045920F1019532764371340195327643714Medline Kit Number/ : UDI/DI each 10195327643713, UDI/DI case 40195327643714, Lot Number: 25CMH298
DYNJ0045920F1019532764371340195327643714Medline Kit Number/ : UDI/DI each 10195327643713, UDI/DI case 40195327643714, Lot Number: 24LMA598
DYNJ0045920F1019532764371340195327643714Medline Kit Number/ : UDI/DI each 10195327643713, UDI/DI case 40195327643714, Lot Number: 24JMH963
DYNJ0045920F1019532764371340195327643714Medline Kit Number/ : UDI/DI each 10195327643713, UDI/DI case 40195327643714, Lot Number: 24IMC899
DYNJ0045920F1019532764371340195327643714Medline Kit Number/ : UDI/DI each 10195327643713, UDI/DI case 40195327643714, Lot Number: 24IMD398
DYNJ0045920F1019532764371340195327643714Medline Kit Number/ : UDI/DI each 10195327643713, UDI/DI case 40195327643714, Lot Number: 24EME289
Amount recalled
2228 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, 5:37 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.