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?

54 of 54 products

Products covered by this recall
Model / numberBarcodesProduct as published
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 24BBF438
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 23LBR516
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 23LBI385
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 23GBW083
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 23GBT137
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 23GBA705
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 23EBT206
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 23BBN853
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 23BBG437
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 23BBG444
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 23BBA852
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 23BBA859
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 22IBR361
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 22IBF066
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 22GBA053
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 22GBA052
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 22GBA054
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 22DBM893
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 22DBS377
CDS983775I1019348998066040193489980661Medline Kit Number/ : UDI/DI 10193489980660 (each), 40193489980661 (case), Lot Number 22OBE639
Amount recalled
2340 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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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:40 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.