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?

12 of 12 products

Products covered by this recall
Model / numberBarcodesProduct as published
CDS984347O1019845931145140198459311452Medline Kit : UDI/DI 10198459311451 (EA) 40198459311452 (CS), Lot Number 25KMD733
CDS984347O1019845931145140198459311452Medline Kit : UDI/DI 10198459311451 (EA) 40198459311452 (CS), Lot Number 25KMC147
CDS984857N1019845935970540198459359706Medline Kit : UDI/DI 10198459359705 (EA) 40198459359706 (CS), Lot Number 25KMJ151
DYNJ0966130K1019845944211740198459442118Medline Kit : UDI/DI 10198459442117 (EA) 40198459442118 (CS), Lot Number 25LMB220
DYNJ0966130K1019845944211740198459442118Medline Kit : UDI/DI 10198459442117 (EA) 40198459442118 (CS), Lot Number 25KME804
DYNJ51440B1019845900423040198459004231Medline Kit : UDI/DI 10198459004230 (EA) 40198459004231 (CS), Lot Number 25KMI445
DYNJ58742J1019845925471040198459254711Medline Kit : UDI/DI 10198459254710 (EA) 40198459254711 (CS), Lot Number 25KMC534
DYNJ63781B1019845954959540198459549596Medline Kit : UDI/DI 10198459549595 (EA) 40198459549596 (CS), Lot Number 25KMB410
DYNJ82751B1019845903915740198459039158Medline Kit : UDI/DI 10198459039157 (EA) 40198459039158 (CS), Lot Number 25LMB068
DYNJ82751B1019845903915740198459039158Medline Kit : UDI/DI 10198459039157 (EA) 40198459039158 (CS), Lot Number 25KMI309
DYNJ82753C1019845944688740198459446888Medline Kit : UDI/DI 10198459446887 (EA) 40198459446888 (CS), Lot Number 25KMC126
DYNJ907206G1019845936802840198459368029Medline Kit : UDI/DI 10198459368028 (EA) 40198459368029 (CS), Lot Number 25KBL336.
Amount recalled
40 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, 5:38 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.