Reported Feb 4, 2026 · Ongoing

Medline medical procedure convenience kits labeled as

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?

9 of 9 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ0660040R1088994222008340889942220084Medline Kit : UDI/DI 10889942220083 (EA) 40889942220084 (CS), Lot Number 25KMG652
DYNJ39225K1019845910225740198459102258Medline Kit : UDI/DI 10198459102257 (EA) 40198459102258 (CS), Lot Number 25JMJ958
DYNJ39225K1019845910225740198459102258Medline Kit : UDI/DI 10198459102257 (EA) 40198459102258 (CS), Lot Number 25KMJ566
DYNJ46620I1019845940400940198459404000Medline Kit : UDI/DI 10198459404009 (EA) 40198459404000 (CS), Lot Number 25KBE927
DYNJ59250I1019845935994140198459359942Medline Kit : UDI/DI 10198459359941 (EA) 40198459359942 (CS), Lot Number 25KMB767
DYNJ65980J1019845942372740198459423728Medline Kit : UDI/DI 10198459423727 (EA) 40198459423728 (CS), Lot Number 25KMJ630
DYNJ68288A1019532705699540195327056996Medline Kit : UDI/DI 10195327056995 (EA) 40195327056996 (CS), Lot Number 25KMF183
MNS130351065316099048240653160990483Medline Kit : UDI/DI 10653160990482 (EA) 40653160990483 (CS), Lot Number 25KME754
PHS41746D1019845943882040198459438821Medline Kit : UDI/DI 10198459438820 (EA) 40198459438821 (CS), Lot Number 25KMD226.
Amount recalled
66 units

This recall covers 15 products

The agency filed one notice per product. You are reading one of them; the other 14 are below.

2 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.

This product could cause temporary or reversible health problems — stop using it.

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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, 6:17 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.