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?

34 of 34 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ19974P1019845913819540198459138196Medline Kit : UDI/DI 10198459138195 (EA) 40198459138196 (CS), Lot Number 25KMB830
DYNJ19974P1019845913819540198459138196Medline Kit : UDI/DI 10198459138195 (EA) 40198459138196 (CS), Lot Number 25KMB831
DYNJ20027K1019845922895740198459228958Medline Kit : UDI/DI 10198459228957 (EA) 40198459228958 (CS), Lot Number 25KMG395
DYNJ20027K1019845922895740198459228958Medline Kit : UDI/DI 10198459228957 (EA) 40198459228958 (CS), Lot Number 25KMH132
DYNJ20468J1019532702433840195327024339Medline Kit : UDI/DI 10195327024338 (EA) 40195327024339 (CS), Lot Number 25KMF540
DYNJ25763N1019845913821840198459138219Medline Kit : UDI/DI 10198459138218 (EA) 40198459138219 (CS), Lot Number 25KMH134
DYNJ25763O1019845960365540198459603656Medline Kit : UDI/DI 10198459603655 (EA) 40198459603656 (CS), Lot Number 25KMI209
DYNJ32836B1019532703736940195327037360Medline Kit : UDI/DI 10195327037369 (EA) 40195327037360 (CS), Lot Number 25KBF167
DYNJ43272K1019845925713140198459257132Medline Kit : UDI/DI 10198459257131 (EA) 40198459257132 (CS), Lot Number 25KME892
DYNJ43976C1019348980669440193489806695Medline Kit : UDI/DI 10193489806694 (EA) 40193489806695 (CS), Lot Number 25KMG962
DYNJ46939Q1019845940404740198459404048Medline Kit : UDI/DI 10198459404047 (EA) 40198459404048 (CS), Lot Number 25JDA437
DYNJ46939Q1019845940404740198459404048Medline Kit : UDI/DI 10198459404047 (EA) 40198459404048 (CS), Lot Number 25LDA059
DYNJ49688C1019845915501740198459155018Medline Kit : UDI/DI 10198459155017 (EA) 40198459155018 (CS), Lot Number 25KMG180
DYNJ51347N1019845938642840198459386429Medline Kit : UDI/DI 10198459386428 (EA) 40198459386429 (CS), Lot Number 25JBW506
DYNJ54081F1019845917241040198459172411Medline Kit : UDI/DI 10198459172410 (EA) 40198459172411 (CS), Lot Number 25KMB295
DYNJ58864B1019845934696540198459346966Medline Kit : UDI/DI 10198459346965 (EA) 40198459346966 (CS), Lot Number 25JBW678
DYNJ59313B1019532724833840195327248339Medline Kit : UDI/DI 10195327248338 (EA) 40195327248339 (CS), Lot Number 25JMJ736
DYNJ61095F1019845922856840198459228569Medline Kit : UDI/DI 10198459228568 (EA) 40198459228569 (CS), Lot Number 25KMC402
DYNJ62065A1019348927347240193489273473Medline Kit : UDI/DI 10193489273472 (EA) 40193489273473 (CS), Lot Number 25KMI773
DYNJ64174A1019845907636740198459076368Medline Kit : UDI/DI 10198459076367 (EA) 40198459076368 (CS), Lot Number 25LMB281
Amount recalled
456 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.

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, 5:41 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.