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
| Model / number | Product as published |
|---|---|
60130527 | MTO,135,YELLOW,MICRO,SPK-MAIMONIDES |
65111341 | MTO,ANGIO,DOUBLE,SPIKE,KIT,KENNEDY HLTH |
65232486 | MTO,ANGIO,SINGLE,SPIKE,KIT |
65071193 | MTO,ANGIO,SINGLE,SPIKE,KIT,GOOD,SAM |
600604422 | MTO,NEURO,FLUSH,SPIKE,KIT,BLUE,FLORIDA |
60100045 | MTO,NEURO,KIT,-,JERSEY,SHORE PG |
650801715 | MTO,RADIOLOGY,KIT,HAMOT MED CEN |
60232481 | MTS,135,CDS,IV,TUBE-JEFFERSON UNIV. |
60120583 | MTS,135,YELLOW,MICRO,SPIKE,LUTHERAN MED |
601403920 | MTS,ANGIO,NEURO,KIT,NORTH SHORE UNIV |
62140602 | MTS,CUST. FILTER-NEWYORK UNIVERSITY |
602301614 | MTS,INTERV,NEURO,KIT-WESTCHESTER,MC |
6010771601 | MTS,NEU,NORTH SHORE HOSPITAL |
600602914 | MTS,NEURO,KIT |
601400111 | MTS,NEURO,KIT,2,NEWENGLAND MED CTR |
600604423 | MTS,NEURO,KIT,YLW&RED,FLORIDA HOSP |
60110552 | MTS,NEURO,KIT-JOHN,F,KENNEDY MED CENTER |
60150035 | MTS,NEURO,KIT-OVERLOOK HOSPITAL PG |
60182723 | MTS,NEURO,SPIKE,KIT,CAPITAL HLTHSYS-FULD |
602500214 | MTS,NEURO-RADIOLOGY,KIT-YALE-NEWHAVEN |
- Lot codes and dates
54 of 54 products
Products covered by this recall # Barcodes Product as published 1 101934890464652019348904646260130527 UDI-D:10193489046465(each), 20193489046462(case), Lot Number:0000133032 2 101934890613142019348906131165111341 UDI-D:10193489061314(each), 20193489061311(case), Lot Number:0000129541 3 101934890613142019348906131165111341 UDI-D:10193489061314(each), 20193489061311(case), Lot Number:0000134701 4 101934890639502019348906395765232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000129544 5 101934890639502019348906395765232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000128715 6 101934890639502019348906395765232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000133060 7 101934890639502019348906395765232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000131657 8 101934890639502019348906395765232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000135723 9 101934890639502019348906395765232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000135294 10 101934890609042019348906090165071193 UDI-D:10193489060904(each), 20193489060901(case), Lot Number:0000130171 11 1019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000135606 12 1019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000134729 13 1019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000137115 14 1019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000130833 15 1019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000131669 16 1019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000129513 17 1019348907022420193489070221600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000128721 18 101934890449283019348904492260100045 UDI-D:10193489044928(each), 30193489044922(case), Lot Number:0000129523 19 101934890449283019348904492260100045 UDI-D:10193489044928(each), 30193489044922(case), Lot Number:0000132393 20 101934890449283019348904492260100045 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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