Reported May 6, 2026 · Ongoing

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

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. NEURO PACK
    • Medline kit number/SKU DYNJ64479
    • 2. CRANIO/NEURO/SPINE
    • Medline kit number/SKU DYNJ901072D
Lot codes and dates

6 of 6 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ86657A1019845943167840198459431679Medline Kit Number/ , UDI/DI each 10198459431678, UDI/DI case 40198459431679, Lot Number: 26ABM977
DYNJ86657A1019845943167840198459431679Medline Kit Number/ , UDI/DI each 10198459431678, UDI/DI case 40198459431679, Lot Number: 25KBM387
DYNJ86657A1019845943167840198459431679Medline Kit Number/ , UDI/DI each 10198459431678, UDI/DI case 40198459431679, Lot Number: 25IBG995
DYNJ86657A1019845943167840198459431679Medline Kit Number/ , UDI/DI each 10198459431678, UDI/DI case 40198459431679, Lot Number: 25GBW704
DYNJT32701019845932223540198459322236Medline Kit Number/ , UDI/DI each 10198459322235, UDI/DI case 40198459322236, Lot Number: 26AMF231
DYNJT32701019845932223540198459322236Medline Kit Number/ , UDI/DI each 10198459322235, UDI/DI case 40198459322236, Lot Number: 25GMC304.
Amount recalled
413 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:53 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.