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?

84 of 84 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ9080971019348997384640193489973847Medline Kit Number, : UDI/DI 10193489973846 (each), 40193489973847 (case), Lot Number 23FBQ975
DYNJ9080971019348997384640193489973847Medline Kit Number, : UDI/DI 10193489973846 (each), 40193489973847 (case), Lot Number 23FBF166
DYNJ9080971019348997384640193489973847Medline Kit Number, : UDI/DI 10193489973846 (each), 40193489973847 (case), Lot Number 23DBM780
DYNJ9080971019348997384640193489973847Medline Kit Number, : UDI/DI 10193489973846 (each), 40193489973847 (case), Lot Number 22KBM832
DYNJ9080971019348997384640193489973847Medline Kit Number, : UDI/DI 10193489973846 (each), 40193489973847 (case), Lot Number 22JBY524
DYNJ9080971019348997384640193489973847Medline Kit Number, : UDI/DI 10193489973846 (each), 40193489973847 (case), Lot Number 22GBR089
DYNJ9080971019348997384640193489973847Medline Kit Number, : UDI/DI 10193489973846 (each), 40193489973847 (case), Lot Number 22FBR153
DYNJ9080971019348997384640193489973847Medline Kit Number, : UDI/DI 10193489973846 (each), 40193489973847 (case), Lot Number 22FBC633
DYNJ9080971019348997384640193489973847Medline Kit Number, : UDI/DI 10193489973846 (each), 40193489973847 (case), Lot Number 22EBB478
DYNJ9080971019348997384640193489973847Medline Kit Number, : UDI/DI 10193489973846 (each), 40193489973847 (case), Lot Number 22BBX706
DYNJ9080971019348997384640193489973847Medline Kit Number, : UDI/DI 10193489973846 (each), 40193489973847 (case), Lot Number 22BBU902
DYNJ9080971019348997384640193489973847Medline Kit Number, : UDI/DI 10193489973846 (each), 40193489973847 (case), Lot Number 22ABN864
DYNJ9080971019348997384640193489973847Medline Kit Number, : UDI/DI 10193489973846 (each), 40193489973847 (case), Lot Number 21IBO640
DYNJ908097A1019532750707740195327507078Medline Kit Number, : UDI/DI 10195327507077 (each), 40195327507078 (case), Lot Number 24EBC216
DYNJ908097A1019532750707740195327507078Medline Kit Number, : UDI/DI 10195327507077 (each), 40195327507078 (case), Lot Number 24CBU878
DYNJ908097A1019532750707740195327507078Medline Kit Number, : UDI/DI 10195327507077 (each), 40195327507078 (case), Lot Number 23LBV779
DYNJ908097A1019532750707740195327507078Medline Kit Number, : UDI/DI 10195327507077 (each), 40195327507078 (case), Lot Number 23JBV724
DYNJ908097A1019532750707740195327507078Medline Kit Number, : UDI/DI 10195327507077 (each), 40195327507078 (case), Lot Number 23JBQ243
DYNJ908097A1019532750707740195327507078Medline Kit Number, : UDI/DI 10195327507077 (each), 40195327507078 (case), Lot Number 23JBQ188
DYNJ908097A1019532750707740195327507078Medline Kit Number, : UDI/DI 10195327507077 (each), 40195327507078 (case), Lot Number 23IBS778
Amount recalled
3521 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, 6:20 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.