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?

52 of 52 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ9122711019845968832440198459688325Medline Kit Number/ : UDI/DI 10198459688324 (each), 40198459688325 (case), Lot Number 26CBQ109
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 25FBO720
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 24KBO387
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 24KBO015
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 24KBD819
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 24KBA736
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 24FBG144
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 24DBO838
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 24BBC453
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 24ABM118
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 23KBS950
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 23IBC670
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 22LBN883
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 22KBF121
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 22IBN293
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 22FBO695
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 22OBH349
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 21JBY498
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 21JBY507
DYNJ31204D1019348995799040193489957991Medline Kit Number/ : UDI/DI 10193489957990 (each), 40193489957991 (case), Lot Number 21JBH105
Amount recalled
1248 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, 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.