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?

29 of 29 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ0275635M1019845946479940198459464790Medline Kit : UDI/DI 10198459464799 (EA) 40198459464790 (CS), Lot Number 25KMH120
DYNJ0395037X1019845960055540198459600556Medline Kit : UDI/DI 10198459600555 (EA) 40198459600556 (CS), Lot Number 25LMB119
DYNJ04809N1019845944090840198459440909Medline Kit : UDI/DI 10198459440908 (EA) 40198459440909 (CS), Lot Number 25KMF969
DYNJ0565499AN1019532731835240195327318353Medline Kit : UDI/DI 10195327318352 (EA) 40195327318353 (CS), Lot Number 25JMF339
DYNJ0565499AN1019532731835240195327318353Medline Kit : UDI/DI 10195327318352 (EA) 40195327318353 (CS), Lot Number 25LMB019
DYNJ27164Q1019845913810240198459138103Medline Kit : UDI/DI 10198459138102 (EA) 40198459138103 (CS), Lot Number 25KMJ742
DYNJ40221G1019845944851540198459448516Medline Kit : UDI/DI 10198459448515 (EA) 40198459448516 (CS), Lot Number 25KME669
DYNJ45311J1019845925567040198459255671Medline Kit : UDI/DI 10198459255670 (EA) 40198459255671 (CS), Lot Number 25KMI080
DYNJ46330C1088994249006640889942490067Medline Kit : UDI/DI 10889942490066 (EA) 40889942490067 (CS), Lot Number 25KMD795
DYNJ48980M1019532753369440195327533695Medline Kit : UDI/DI 10195327533694 (EA) 40195327533695 (CS), Lot Number 25KMC459
DYNJ52995F1019532763977840195327639779Medline Kit : UDI/DI 10195327639778 (EA) 40195327639779 (CS), Lot Number 25KME064
DYNJ56483L1019532751814140195327518142Medline Kit : UDI/DI 10195327518141 (EA) 40195327518142 (CS), Lot Number 25LMB049
DYNJ61200B1019532760426440195327604265Medline Kit : UDI/DI 10195327604264 (EA) 40195327604265 (CS), Lot Number 25KBE867
DYNJ661501019348931755840193489317559Medline Kit : UDI/DI 10193489317558 (EA) 40193489317559 (CS), Lot Number 25KMC057
DYNJ666301019348936828440193489368285Medline Kit : UDI/DI 10193489368284 (EA) 40193489368285 (CS), Lot Number 25KMG435
DYNJ69065F1019845922661840198459226619Medline Kit : UDI/DI 10198459226618 (EA) 40198459226619 (CS), Lot Number 25KMI293
DYNJ69113C1019845917022540198459170226Medline Kit : UDI/DI 10198459170225 (EA) 40198459170226 (CS), Lot Number 25JMJ726
DYNJ69401D1019845918367640198459183677Medline Kit : UDI/DI 10198459183676 (EA) 40198459183677 (CS), Lot Number 25KMJ106
DYNJ81013D1019845954770640198459547707Medline Kit : UDI/DI 10198459547706 (EA) 40198459547707 (CS), Lot Number 25LDA122
DYNJ84275A1019845924017140198459240172Medline Kit : UDI/DI 10198459240171 (EA) 40198459240172 (CS), Lot Number 25LMB546
Amount recalled
117 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, 7:37 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.