Reported May 6, 2026 · Ongoing

Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. MICRODISECTOMY PACK, Medline…

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
  • labeled as follows
    • 1. MICRODISECTOMY PACK
    • Medline Kit Number/SKU DYNJ80585B
    • 2. MICRODISECTOMY PACK
    • Medline Kit Number/SKU DYNJ80585C
    • 3
    • MICRODISECTOMY PACK
    • Medline Kit Number/SKU DYNJ80585D
Lot codes and dates

15 of 15 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ80585B1019532721115840195327211159Medline Kit Number/ : UDI/DI each 10195327211158, UDI/DI case 40195327211159, Lot Number: 22GBV101
DYNJ80585B1019532721115840195327211159Medline Kit Number/ : UDI/DI each 10195327211158, UDI/DI case 40195327211159, Lot Number: 24IBG473
DYNJ80585C1019845915475140198459154752Medline Kit Number/ : UDI/DI each 10198459154751, UDI/DI case 40198459154752, Lot Number: 25EBT656
DYNJ80585C1019845915475140198459154752Medline Kit Number/ : UDI/DI each 10198459154751, UDI/DI case 40198459154752, Lot Number: 25DBN421
DYNJ80585C1019845915475140198459154752Medline Kit Number/ : UDI/DI each 10198459154751, UDI/DI case 40198459154752, Lot Number: 25CBN640
DYNJ80585C1019845915475140198459154752Medline Kit Number/ : UDI/DI each 10198459154751, UDI/DI case 40198459154752, Lot Number: 25BBL172
DYNJ80585C1019845915475140198459154752Medline Kit Number/ : UDI/DI each 10198459154751, UDI/DI case 40198459154752, Lot Number: 25BBD651
DYNJ80585C1019845915475140198459154752Medline Kit Number/ : UDI/DI each 10198459154751, UDI/DI case 40198459154752, Lot Number: 25ABA455
DYNJ80585C1019845915475140198459154752Medline Kit Number/ : UDI/DI each 10198459154751, UDI/DI case 40198459154752, Lot Number: 24KBO858
DYNJ80585C1019845915475140198459154752Medline Kit Number/ : UDI/DI each 10198459154751, UDI/DI case 40198459154752, Lot Number: 24JBH693
DYNJ80585D1019845938933740198459389338Medline Kit Number/ : UDI/DI each 10198459389337, UDI/DI case 40198459389338, Lot Number: 26ABH754
DYNJ80585D1019845938933740198459389338Medline Kit Number/ : UDI/DI each 10198459389337, UDI/DI case 40198459389338, Lot Number: 25LBA242
DYNJ80585D1019845938933740198459389338Medline Kit Number/ : UDI/DI each 10198459389337, UDI/DI case 40198459389338, Lot Number: 25HBT362
DYNJ80585D1019845938933740198459389338Medline Kit Number/ : UDI/DI each 10198459389337, UDI/DI case 40198459389338, Lot Number: 25GBL430
DYNJ80585D1019845938933740198459389338Medline Kit Number/ : UDI/DI each 10198459389337, UDI/DI case 40198459389338, Lot Number: 25FBT402.
Amount recalled
924 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, 7:35 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.