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?

60 of 60 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ908483A1019532719188740195327191888Medline Kit Number/ : UDI/DI 10195327191887, (each) 40195327191888, (case), Lot Number 22HMA818
DYNJ908483A1019532719188740195327191888Medline Kit Number/ : UDI/DI 10195327191887, (each) 40195327191888, (case), Lot Number 22GMG188
DYNJ908483B1019532728776440195327287765Medline Kit Number/ : UDI/DI 10195327287764, (each) 40195327287765, (case), Lot Number 23FMB021
DYNJ908483B1019532728776440195327287765Medline Kit Number/ : UDI/DI 10195327287764, (each) 40195327287765, (case), Lot Number 23CMB395
DYNJ908483B1019532728776440195327287765Medline Kit Number/ : UDI/DI 10195327287764, (each) 40195327287765, (case), Lot Number 23BMF105
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 25BMG115
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 24KMG981
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 24KMG043
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 24KME988
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 24JMC883
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 24HMG291
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 24GMG957
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 24GMC708
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 24EMD960
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 24EMD976
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 24CMC199
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 23LMH271
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 23LMC861
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 23JMI184
DYNJ908483C1019532743211940195327432110Medline Kit Number/ : UDI/DI 10195327432119, (each) 40195327432110, (case), Lot Number 23JMC583
Amount recalled
1432 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.

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.

Free recall alerts

Get alerted about new Medline Industries, LP recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.

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, 7:35 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.