Reported May 6, 2026 · Ongoing

Medline and Centurion medical procedure kits, containing Medline Neuro Sponges (1229 in total), HEAD & NECK TRAY,…

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 and Centurion medical procedure kits, containing Medline Neuro Sponges (1229 in total), HEAD & NECK TRAY, SINUS, SMR, etc.
Lot codes and dates

284 of 284 products

Products covered by this recall
Model / numberBarcodesProduct as published
AM310B1019348924212640193489242127Medline Kit Number/ : UDI/DI each 10193489242126, UDI/DI case 40193489242127, Lot Number: 20XBG776
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 23JBF547
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 23GBK604
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 23DBO915
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 23DBD581
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 23ABP476
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 23ABD648
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 22LBE888
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 22HBL188
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 22HBF976
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 22FBN678
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 22DBK641
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 22BBU367
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 22ABD373
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 21JBC146
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 21IBA072
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 21FBN768
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 21FBB075
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 21EBI490
CDS980579D1088994213371040889942133711Medline Kit Number/ : UDI/DI each 10889942133710, UDI/DI case 40889942133711, Lot Number: 24CBU365
Amount recalled
486946 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, 6:21 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.