Reported Jun 24, 2026 · Ongoing

MEDLINE Medical Procedure 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?

130 of 130 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ47625B1088994218258940889942182580Medline Kit Number/ , UDI/DI 10889942182589 (each), 40889942182580 (case), Lot Number 21LBI584
DYNJ9122191019845967604840198459676049Medline Kit Number/ , UDI/DI 10198459676048 (each), 40198459676049 (case), Lot Number 26BBQ085
DYNJ907033B1019532720598040195327205981Medline Kit Number/ , UDI/DI 10195327205980 (each), 40195327205981 (case), Lot Number 23BBK437
DYNJ907033B1019532720598040195327205981Medline Kit Number/ , UDI/DI 10195327205980 (each), 40195327205981 (case), Lot Number 22LBP927
DYNJ907033B1019532720598040195327205981Medline Kit Number/ , UDI/DI 10195327205980 (each), 40195327205981 (case), Lot Number 22KBA970
DYNJ907033B1019532720598040195327205981Medline Kit Number/ , UDI/DI 10195327205980 (each), 40195327205981 (case), Lot Number 22JBH943
DYNJ907033B1019532720598040195327205981Medline Kit Number/ , UDI/DI 10195327205980 (each), 40195327205981 (case), Lot Number 22HBR879
DYNJ68663B1019532740888640195327408887Medline Kit Number/ , UDI/DI 10195327408886 (each), 40195327408887 (case), Lot Number 25ABD038
DYNJ68663B1019532740888640195327408887Medline Kit Number/ , UDI/DI 10195327408886 (each), 40195327408887 (case), Lot Number 24IBP599
DYNJ68663B1019532740888640195327408887Medline Kit Number/ , UDI/DI 10195327408886 (each), 40195327408887 (case), Lot Number 24HBT938
DYNJ68663B1019532740888640195327408887Medline Kit Number/ , UDI/DI 10195327408886 (each), 40195327408887 (case), Lot Number 24GBB724
DYNJ68663B1019532740888640195327408887Medline Kit Number/ , UDI/DI 10195327408886 (each), 40195327408887 (case), Lot Number 24DBK110
DYNJ68663B1019532740888640195327408887Medline Kit Number/ , UDI/DI 10195327408886 (each), 40195327408887 (case), Lot Number 24ABN322
DYNJ68663B1019532740888640195327408887Medline Kit Number/ , UDI/DI 10195327408886 (each), 40195327408887 (case), Lot Number 23LBB050
DYNJ68663B1019532740888640195327408887Medline Kit Number/ , UDI/DI 10195327408886 (each), 40195327408887 (case), Lot Number 23KBB963
DYNJ68663B1019532740888640195327408887Medline Kit Number/ , UDI/DI 10195327408886 (each), 40195327408887 (case), Lot Number 23HBG577
DYNJ68663B1019532740888640195327408887Medline Kit Number/ , UDI/DI 10195327408886 (each), 40195327408887 (case), Lot Number 23GBV662
DYNJ68663B1019532740888640195327408887Medline Kit Number/ , UDI/DI 10195327408886 (each), 40195327408887 (case), Lot Number 23FBC135
DYNJ68663B1019532740888640195327408887Medline Kit Number/ , UDI/DI 10195327408886 (each), 40195327408887 (case), Lot Number 23EBI988
DYNJ14099F1019348935250440193489352505Medline Kit Number/ , UDI/DI 10193489352504 (each), 40193489352505 (case), Lot Number 23EMG547
Amount recalled
24388 units

This recall covers 64 products

The agency filed one notice per product. You are reading one of them; the other 63 are below.

51 more are in the archive.

Where it was sold

Why it was recalled

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

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

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By hazard

Other recalls from Medline Industries, LP

36 in total.

Where it was distributed

All recall categories · Browse the whole archive

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:33 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.