Reported Dec 4, 2024 · Ongoing

MEDLINE procedure kits labeled as follows

MEDLINE INDUSTRIES, LP - Northfield

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 - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

MEDLINE procedure kits labeled as follows

5 of 5 products

Products covered by this recall
Model / numberProduct as published
PAIN1069BCONT EPI 20G W/HUSTEAD
PAIN1941CSE TRAY
PAIN9023TRAY CON EPID 20G NYL W/TUOHY
PAIN1281TRAY, CONT EPI 20G NYL W/ HUST
PAIN9024TRAY, CONT EPI 20G NYL W/ HUST
Lot codes and dates

5 of 5 products

Products covered by this recall
#BarcodesProduct as published
11088994275738140889942757382PAIN1069B UDI-DI: 10889942757381 (each) 40889942757382 (case), Lot Numbers: 22GLA433, 23CLA257
21019532736541740195327365418PAIN1941 UDI-DI: 10195327365417 (each) 40195327365418(case), Lot Numbers: 23ELB081
31088994244871540889942448716PAIN9023 UDI-DI: 10889942448715(each) 40889942448716 (case), Lot Numbers: 22GLA470, 22ILA287
41088827774840840888277748409PAIN1281 UDI-DI: 10888277748408(each) 40888277748409(case), Lot Numbers: 22FLA647
51088994244870840889942448709PAIN9024 UDI-DI: 10889942448708(each) 40889942448709(case), Lot Numbers: 22FLA675, 22GLA241, 22HLB225, 22ILA288
Amount recalled
3744 units

This recall covers 12 products

The agency filed one notice per product. You are reading one of them; the other 11 are below.

Where it was sold

  • Nationwide

Why it was recalled

The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.

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

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 5:43 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.