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?
69 of 69 products
| Model / number | Barcodes | Product as published |
|---|---|---|
ACC010270A | 1088994221982740889942219828 | Medline Kit : UDI/DI 10889942219827 (EA) 40889942219828 (CS), Lot Number 25LDA153 |
ACC010690 | 1019532743330740195327433308 | Medline Kit : UDI/DI 10195327433307 (EA) 40195327433308 (CS), Lot Number 25LDA088 |
ACC011073 | 1019845956933340198459569334 | Medline Kit : UDI/DI 10198459569333 (EA) 40198459569334 (CS), Lot Number 25LDA072 |
DYNJ00282Q | 1019532741202940195327412020 | Medline Kit : UDI/DI 10195327412029 (EA) 40195327412020 (CS), Lot Number 25KMC904 |
DYNJ00282Q | 1019532741202940195327412020 | Medline Kit : UDI/DI 10195327412029 (EA) 40195327412020 (CS), Lot Number 25LMA071 |
DYNJ0101360K | 1019532766206640195327662067 | Medline Kit : UDI/DI 10195327662066 (EA) 40195327662067 (CS), Lot Number 25KMC709 |
DYNJ0220136S | 1019845956607340198459566074 | Medline Kit : UDI/DI 10198459566073 (EA) 40198459566074 (CS), Lot Number 25KMB403 |
DYNJ0220136S | 1019845956607340198459566074 | Medline Kit : UDI/DI 10198459566073 (EA) 40198459566074 (CS), Lot Number 25JMF503 |
DYNJ0376635Q | 1019845942259140198459422592 | Medline Kit : UDI/DI 10198459422591 (EA) 40198459422592 (CS), Lot Number 25KMH121 |
DYNJ0376635Q | 1019845942259140198459422592 | Medline Kit : UDI/DI 10198459422591 (EA) 40198459422592 (CS), Lot Number 25KMF780 |
DYNJ0460768T | 1019845946680940198459466800 | Medline Kit : UDI/DI 10198459466809 (EA) 40198459466800 (CS), Lot Number 25KMH789 |
DYNJ0509186J | 1019845911762640198459117627 | Medline Kit : UDI/DI 10198459117626 (EA) 40198459117627 (CS), Lot Number 25KME895 |
DYNJ0578815W | 1019845946689240198459466893 | Medline Kit : UDI/DI 10198459466892 (EA) 40198459466893 (CS), Lot Number 25JMJ695 |
DYNJ0610290T | 1019845902155840198459021559 | Medline Kit : UDI/DI 10198459021558 (EA) 40198459021559 (CS), Lot Number 25KMC723 |
DYNJ0753436P | 1019845946685440198459466855 | Medline Kit : UDI/DI 10198459466854 (EA) 40198459466855 (CS), Lot Number 25KMJ740 |
DYNJ0890502R | 1019845943109840198459431099 | Medline Kit : UDI/DI 10198459431098 (EA) 40198459431099 (CS), Lot Number 25KME522 |
DYNJ28212L | 1019348932211840193489322119 | Medline Kit : UDI/DI 10193489322118 (EA) 40193489322119 (CS), Lot Number 25KBE916 |
DYNJ31341P | 1019845906935240198459069353 | Medline Kit : UDI/DI 10198459069352 (EA) 40198459069353 (CS), Lot Number 25KMA795 |
DYNJ37615J | 1019532756088140195327560882 | Medline Kit : UDI/DI 10195327560881 (EA) 40195327560882 (CS), Lot Number 25KDB706 |
DYNJ39215N | 1019845910224040198459102241 | Medline Kit : UDI/DI 10198459102240 (EA) 40198459102241 (CS), Lot Number 25KMH027 |
- Amount recalled
- 857 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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