Reported Sep 30, 2026 · Ongoing · Updated Oct 6, 2026

Medline Convenience Kits

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 Convenience Kits

7 of 7 products

Products covered by this recall
Model / numberProduct as published
DYNJ39218IMAJOR NEURO VCH
DYNJ41246FNEURO PACK-LF
DYNJ47487ACRANIOTOMY PACK (CRSJE)227-LF
DYNJ57233JMAJOR NEURO PACK
DYNJ82388ANEURO
DYNJ86656NEURO PACK
DYNJ904549GNEURO ACD
Lot codes and dates

7 of 7 products

Products covered by this recall
#BarcodesProduct as published
11019532711201140195327112012Lot Number: 22HMA400; 2) DYNJ41246F, UDI-DI: 10195327112011(each), 40195327112012(case)
21088994210624040889942106241Lot Number: 23GBS783; 3) DYNJ47487A, UDI-DI: 10889942106240(each), 40889942106241(case)
31019845972302540198459723026Lot Number: 22HMD080; 4) DYNJ57233J, UDI-DI: 10198459723025(each), 40198459723026(case)
41019532748274940195327482740Lot Number: 26CMG313; 5) DYNJ82388A, UDI-DI: 10195327482749(each), 40195327482740(case)
51019532766315540195327663156Lot Number: 25KMB622; 6) DYNJ86656, UDI-DI: 10195327663155(each), 40195327663156(case)
61019348983268640193489832687Lot Number: 24EDB134; 7) DYNJ904549G, UDI-DI: 10193489832686(each), 40193489832687(case)
7Lot Number: 23IBL172
Amount recalled
234 kits

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

  • Nationwide

Why it was recalled

The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could require medical intervention, such as neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.

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 Nov 4, 1:46 AM 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.