Reported May 6, 2026 · Ongoing

Medline medical procedure kits, containing Medline Neuro Sponges (1050 in total), BIOBURDEN TEST KIT, NEURO, ROBOTIC,…

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?

  • Medline medical procedure kits, containing Medline Neuro Sponges (1050 in total), BIOBURDEN TEST KIT, NEURO, ROBOTIC, ACDF, ENT, etc.
Lot codes and dates

283 of 283 products

Products covered by this recall
Model / numberBarcodesProduct as published
BIOB1101088994275804340889942758044Medline Kit Number/ : UDI/DI each 10889942758043, UDI/DI case 40889942758044, Lot Number: 24HBM826
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 23KBK939
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 23JBD164
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 23HBJ252
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 23EBV328
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 23DBD983
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 23BBR624
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 23BBM647
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 23BBB199
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 23ABR879
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 23ABK516
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 22KBO464
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 22IBD725
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 22FBH811
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 22DBG358
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 22CBS385
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 22ABG822
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 24CBK278
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 24CBG921
CDS780056M1019532704556240195327045563Medline Kit Number/ : UDI/DI each 10195327045562, UDI/DI case 40195327045563, Lot Number: 24BBM090
Amount recalled
263739 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, 5:41 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.