Class I — the FDA judged there is a reasonable probability that use of the product would cause serious harm or death.
This is the FDA's risk judgment for this recall. It describes the potential of the product as a category — it does not establish that any specific unit harmed anyone.
Medline Fluid Delivery Set with Drip Chamber: 1) MTO,135,YELLOW,MICRO,SPK-MAIMONIDES, Item Number: 60130527; 2) MTO,ANGIO,DOUBLE,SPIKE,KIT,KENNEDY HLTH, Item Number: 65111341; 3) MTO,ANGIO,SINGLE,SPIKE,KIT, Item Number: 65232486; 4) MTO,ANGIO,SINGLE,SPIKE,KIT,GOOD,SAM, Item Number: 65071193; 5) MTO,NEURO,FLUSH,SPIKE,KIT,BLUE,FLORIDA, Item Number: 600604422; 6) MTO,NEURO,KIT,-,JERSEY,SHORE PG, Item Number: 60100045; 7) MTO,RADIOLOGY,KIT,HAMOT MED CEN, Item Number: 650801715; 8) MTS,135,CDS,IV,TUBE-JEFFERSON UNIV., Item Number: 60232481; 9) MTS,135,YELLOW,MICRO,SPIKE,LUTHERAN MED, Item Number: 60120583; 10) MTS,ANGIO,NEURO,KIT,NORTH SHORE UNIV, Item Number: 601403920; 11) MTS,CUST. FILTER-NEWYORK UNIVERSITY, Item Number: 62140602; 12) MTS,INTERV,NEURO,KIT-WESTCHESTER,MC, Item Number: 602301614; 13) MTS,NEU,NORTH SHORE HOSPITAL, Item Number: 6010771601; 14) MTS,NEURO,KIT, Item Number: 600602914; 15) MTS,NEURO,KIT,2,NEWENGLAND MED CTR, Item Number: 601400111; 16) MTS,NEURO,KIT,YLW&RED,FLORIDA HOSP, Item Number: 600604423; 17) MTS,NEURO,KIT-JOHN,F,KENNEDY MED CENTER, Item Number: 60110552; 18) MTS,NEURO,KIT-OVERLOOK HOSPITAL PG, Item Number: 60150035; 19) MTS,NEURO,SPIKE,KIT,CAPITAL HLTHSYS-FULD, Item Number: 60182723; 20) MTS,NEURO-RADIOLOGY,KIT-YALE-NEWHAVEN, Item Number: 602500214; 21) MTS,STROKE/EMBO,KIT,NORTH SHORE UNIV, Item Number: 601403921; 22) MTS,YELLOW,/,RED,MULTILINE,KIT,MAIMONIDE, Item Number: 601305210; 23) MTS,YELLOW,/,RED,MULTILINE,KIT,MAIMONIDE, Item Number: 601400110;
Why it was recalled
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.
Is your unit affected?
The recall covers only the specific lots or serial numbers the FDA listed. Enter the lot or serial number from your product's label and we'll check it against that list.
A match means your unit may be covered — stop and call your pharmacist before doing anything. No match suggests it isn't covered, but confirm anyway: code formats vary and lists can be incomplete. Your unit not being listed does not guarantee it is safe, and being listed does not mean you have been harmed.
Show the FDA's listed lot / code information
1) 60130527 UDI-D:10193489046465(each), 20193489046462(case), Lot Number:0000133032; 2) 65111341 UDI-D:10193489061314(each), 20193489061311(case), Lot Number:0000129541; 3) 65111341 UDI-D:10193489061314(each), 20193489061311(case), Lot Number:0000134701; 4) 65232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000129544; 5) 65232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000128715; 6) 65232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000133060; 7) 65232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000131657; 8) 65232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000135723; 9) 65232486 UDI-D:10193489063950(each), 20193489063957(case), Lot Number:0000135294; 10) 65071193 UDI-D:10193489060904(each), 20193489060901(case), Lot Number:0000130171; 11) 600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000135606; 12) 600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000134729; 13) 600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000137115; 14) 600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000130833; 15) 600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000131669; 16) 600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000129513; 17) 600604422 UDI-D:10193489070224(each), 20193489070221(case), Lot Number:0000128721; 18) 60100045 UDI-D:10193489044928(each), 30193489044922(case), Lot Number:0000129523; 19) 60100045 UDI-D:10193489044928(each), 30193489044922(case), Lot Number:0000132393; 20) 60100045 UDI-D:10193489044928(each), 30193489044922(case), Lot Number:0000134940; 21) 60100045 UDI-D:10193489044928(each), 30193489044922(case), Lot Number:0000144158; 22) 60100045 UDI-D:10193489044928(each), 30193489044922(case), Lot Number:0000139082; 23) 650801715 UDI-D:10193489075458(each), 20193489075455(case), Lot Number:0000130138; 24) 650801715 UDI-D:10193489075458(each), 20193489075455(case), Lot Number:0000132350; 25) 650801715 UDI-D:10193489075458(each), 20193489075455(case), Lot Number:0000135736; 26) 60232481 UDI-D:10193489053326(each), 30193489053320(case), Lot Number:0000129534; 27) 60120583 UDI-D:10193489045864(each), 30193489045868(case), Lot Number:0000133660; 28) 60120583 UDI-D:10193489045864(each), 30193489045868(case), Lot Number:0000136501; 29) 60120583 UDI-D:10193489045864(each), 30193489045868(case), Lot Number:0000131600; 30) 601403920 UDI-D:10193489071498(each), 30193489071492(case), Lot Number:0000131376; 31) 601403920 UDI-D:10193489071498(each), 30193489071492(case), Lot Number:0000130940; 32) 62140602 UDI-D:10193489057805(each), 30193489057809(case), Lot Number:0000132222; 33) 62140602 UDI-D:10193489057805(each), 30193489057809(case), Lot Number:0000141215; 34) 602301614 UDI-D:10193489072754(each), 30193489072758(case), Lot Number:0000133659; 35) 6010771601 UDI-D:10193489099843(each), 30193489099847(case), Lot Number:0000127859; 36) 600602914 UDI-D:10193489070170(each), 30193489070174(case), Lot Number:0000135717; 37) 600602914 UDI-D:10193489070170(each), 30193489070174(case), Lot Number:0000128447; 38) 601400111 UDI-D:10193489071344(each), 30193489071348(case), Lot Number:0000133121; 39) 601400111 UDI-D:10193489071344(each), 30193489071348(case), Lot Number:0000130573; 40) 600604423 UDI-D:10193489070231(each), 30193489070235(case), Lot Number:0000128607; 41) 600604423 UDI-D:10193489070231(each), 30193489070235(case), Lot Number:0000137751; 42) 60110552 UDI-D:10193489045611(each), 30193489045615(case), Lot Number:0000131878; 43) 60110552 UDI-D:10193489045611(each), 30193489045615(case), Lot Number:0000130577; 44) 60110552 UDI-D:10193489045611(each), 30193489045615(case), Lot Number:0000138084; 45) 60150035 UDI-D:10193489048292(each), 30193489048296(case), Lot Number:0000130187; 46) 60150035 UDI-D:10193489048292(each), 30193489048296(case), Lot Number:0000131883; 47) 60150035 UDI-D:10193489048292(each), 30193489048296(case), Lot Number:0000143095; 48) 60182723 UDI-D:10193489049817(each), 30193489049811(case), Lot Number:0000130988; 49) 602500214 UDI-D:10193489072815(each), 30193489072819(case), Lot Number:0000127874; 50) 601403921 UDI-D:30193489071508(each), 30193489071508(case), Lot Number:0000131619; 51) 601403921 UDI-D:30193489071508(each), 30193489071508(case), Lot Number:0000133025; 52) 601403921 UDI-D:30193489071508(each), 30193489071508(case), Lot Number:0000136559; 53) 601305210 UDI-D:10193489070989(each), 30193489070983(case), Lot Number:0000130984; 54) 601400110 UDI-D:10193489071337(each), 30193489071331(case), Lot Number:0000128757;
Recall status
Ongoing — the recall is still being carried out.
Where it was distributed
US Nationwide Distribution
Recall record
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Product type
- Devices
- Recall number
- Z-0765-2025
- Voluntary / mandated
- Voluntary: Firm initiated
- Initial notification
- Letter
- Origin
- Northfield, IL
- Recall initiated
- 2024-12-16
What to do
Check the lot/code above against your product. To confirm this record and read the FDA's full notice, see the FDA recall page. Before changing anything you take or use, ask your pharmacist or prescriber — this page does not tell you to start or stop any drug or device.
Also available: structured data (JSON-LD) · recall record (JSON)
What this is — and is not
A recall is a recorded FDA enforcement action — the FDA logged that a firm is removing or correcting a product. It does not establish that any specific unit harmed anyone, and causation is not established by a recall. The class above is the FDA's risk judgment for the product category, not a finding about your unit. This page informs and compares; it is not medical advice and never tells you to start or stop a drug or device.
To report a problem you experienced, use
FDA MedWatch.
Verify this record at FDA recalls ·
Recall Z-0765-2025 · Source: openFDA enforcement.