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

23 of 23 products

Products covered by this recall
Model / numberProduct as published
60130527MTO,135,YELLOW,MICRO,SPK-MAIMONIDES
65111341MTO,ANGIO,DOUBLE,SPIKE,KIT,KENNEDY HLTH
65232486MTO,ANGIO,SINGLE,SPIKE,KIT
65071193MTO,ANGIO,SINGLE,SPIKE,KIT,GOOD,SAM
600604422MTO,NEURO,FLUSH,SPIKE,KIT,BLUE,FLORIDA
60100045MTO,NEURO,KIT,-,JERSEY,SHORE PG
650801715MTO,RADIOLOGY,KIT,HAMOT MED CEN
60232481MTS,135,CDS,IV,TUBE-JEFFERSON UNIV.
60120583MTS,135,YELLOW,MICRO,SPIKE,LUTHERAN MED
601403920MTS,ANGIO,NEURO,KIT,NORTH SHORE UNIV
62140602MTS,CUST. FILTER-NEWYORK UNIVERSITY
602301614MTS,INTERV,NEURO,KIT-WESTCHESTER,MC
6010771601MTS,NEU,NORTH SHORE HOSPITAL
600602914MTS,NEURO,KIT
601400111MTS,NEURO,KIT,2,NEWENGLAND MED CTR
600604423MTS,NEURO,KIT,YLW&RED,FLORIDA HOSP
60110552MTS,NEURO,KIT-JOHN,F,KENNEDY MED CENTER
60150035MTS,NEURO,KIT-OVERLOOK HOSPITAL PG
60182723MTS,NEURO,SPIKE,KIT,CAPITAL HLTHSYS-FULD
602500214MTS,NEURO-RADIOLOGY,KIT-YALE-NEWHAVEN
Lot codes and dates

54 of 54 products

Products covered by this recall
#BarcodesProduct as published
1101934890464652019348904646260130527 UDI-D:10193489046465(each), 20193489046462(case), Lot Number:0000133032
2101934890613142019348906131165111341 UDI-D:10193489061314(each), 20193489061311(case), Lot Number:0000129541
3101934890613142019348906131165111341 UDI-D:10193489061314(each), 20193489061311(case), Lot Number:0000134701
4101934890639502019348906395765232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000129544
5101934890639502019348906395765232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000128715
6101934890639502019348906395765232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000133060
7101934890639502019348906395765232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000131657
8101934890639502019348906395765232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000135723
9101934890639502019348906395765232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000135294
10101934890609042019348906090165071193 UDI-D:10193489060904(each), 20193489060901(case), Lot Number:0000130171
111019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000135606
121019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000134729
131019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000137115
141019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000130833
151019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000131669
161019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000129513
171019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000128721
18101934890449283019348904492260100045 UDI-D:10193489044928(each), 30193489044922(case), Lot Number:0000129523
19101934890449283019348904492260100045 UDI-D:10193489044928(each), 30193489044922(case), Lot Number:0000132393
20101934890449283019348904492260100045 UDI-D:10193489044928(each), 30193489044922(case), Lot Number:0000134940
Amount recalled
3930 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.

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.

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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, 6:54 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.