Reported Jan 22, 2025 · Ongoing

Medline Fluid Delivery Set with Drip Chamber

MEDLINE INDUSTRIES, LP - Northfield

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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 Fluid Delivery Set with Drip Chamber

5 of 5 products

Products covered by this recall
Model / numberProduct as published
99000069FDS,135,CHMN,W/F,MLL,RC(2),PG
949000222FDS,135,NV,MICRO-CHAMBER,W/FILTER,BLUE
949000224FDS,135,NV,MICRO-CHAMBER,W/FILTER,GREEN
949000221FDS,135,NV,MICRO-CHAMBER,W/FILTER,RED
949000223FDS,135,NV,MICRO-CHAMBER,W/FILTER,YELLOW
Lot codes and dates

9 of 9 products

Products covered by this recall
#BarcodesProduct as published
11019348906958730193489069581Lot Number:0000128741; 2)99000069UDI-D:10193489069587(each)30193489069581(case)
21019348906958730193489069581Lot Number:0000134505; 3)99000069UDI-D:10193489069587(each)30193489069581(case)
31019348906958730193489069581Lot Number:0000133893; 4)99000069UDI-D:10193489069587(each)30193489069581(case)
41019348906958730193489069581Lot Number:0000135769; 5)99000069UDI-D:10193489069587(each)30193489069581(case)
51019734401855030197344018554Lot Number:0000139596; 6)949000222UDI-D:10197344018550(each)30197344018554(case)
61019734401864230197344018646Lot Number:0000133018; 7)949000224UDI-D:10197344018642(each)30197344018646(case)
71019734401856730197344018561Lot Number:0000136573; 8)949000221UDI-D:10197344018567(each)30197344018561(case)
81019734401854330197344018547Lot Number:0000133036; 9)949000223UDI-D:10197344018543(each)30197344018547(case)
9Lot Number:0000133031
Amount recalled
13,600 units

This recall covers 2 products

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

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

Fluid Delivery Sets were incorrectly assembled with a white macro drip chamber instead of the required grey micro drip chamber. The macro drip chamber delivers three times more fluid per drop than the micro drip chamber.

Using this product could cause serious injury, illness or death — stop using it now.

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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, 5:35 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.