ICU Medical B33034Recalls & reported problems
Icu Medical, Inc. · 12" Smallbore Trifuse Ext Set w/3 MicroClave® (Red, Glow Ring), 0.2 Micron Filter, 3 Clamps, Rotating Luer · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887709005921), received between Jun 22, 2024 and Jul 2, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (2 reports).
188 other recalls cover devices cleared under the same FDA submission (K964435); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 2, 2024Fluid/Blood Leak; Fluid/Blood Leak
THE COMPLAINT/EVENT INVOLVED A 12" SMALLBORE TRIFUSE EXT SET W/3 MICROCLAVE® (RED, GLOW RING), 0.2 MICRON FILTER, 3 CLAMPS, ROTATING LUER. UPON REMOVING THE MEDICATION TUBING OR A SYRINGE FROM THE RED PORT (THAT THE FACILITY USES FOR AN INTRAVENOUS MEDICATION PUSH OR FOR CONNECTION TO MEDICATION TUBING FOR CONTINUOUS INFUSION PURPOSES), THE INNER CLEAR VALVE BECAME STUCK. ALTHOUGH FLUID LEAKAGE WAS NOT NOTICED AT THE TIME, FLUID WAS EVENTUALLY IDENTIFIED ON THE LINEN OF A BED. THERE WAS NO HUMAN HARM ASSOCIATED WITH THIS COMPLAINT/EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19661531 ↗MalfunctionJun 22, 2024Fluid/Blood Leak; Fluid/Blood Leak
THE COMPLAINT/EVENT INVOLVED A 12" SMALLBORE TRIFUSE EXT SET W/3 MICROCLAVE® (RED, GLOW RING), 0.2 MICRON FILTER, 3 CLAMPS, ROTATING LUER. UPON REMOVING THE MEDICATION TUBING OR A SYRINGE FROM THE RED PORT (THAT THE FACILITY USES FOR AN INTRAVENOUS MEDICATION PUSH OR FOR CONNECTION TO MEDICATION TUBING FOR CONTINUOUS INFUSION PURPOSES), THE INNER CLEAR VALVE BECAME STUCK. ALTHOUGH FLUID LEAKAGE WAS NOT NOTICED AT THE TIME, FLUID WAS EVENTUALLY IDENTIFIED ON THE LINEN OF A BED. THERE WAS NO HUMAN HARM ASSOCIATED WITH THIS COMPLAINT/EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19590648 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K964435. One submission often covers many models, so check the product and lot details in each record.
- Z-3163-2026 · May 12, 2026 · Open, ClassifiedIV Sets with drip chambers
- Z-3157-2026 · May 12, 2026 · Open, ClassifiedIV Non-Dedicated Gravity Administration Sets with drip chambers
- Z-0154-2026 · Oct 2, 2025 · Open, ClassifiedIV Administration sets. 23" (58 cm) 150 mL Burette Set (Clave, Shut Off) w/Clave, Luer Lock, REF: B33359; 23" (58 cm) 150 ml Burette Set (w/Shut Off), MicroClave, Clamp, REF: B92
- Z-1721-2022 · Aug 1, 2022 · Open, Classified6.5" (17 cm) Appx 0.84 ml, Smallbore Bifuse Ext Set w/2 MicroClave Clear, 2 Check Valves, Luer Lock;
- Z-0956-2021 · Dec 2, 2020 · Terminated60" (152 cm) Appx 1.9 ml, Smallbore Ext Set w/MicroClave Clear, 1.2 Micron Filter, 2 Clamps, Luer Lock REF MC330174 - Product Usage: The intravascular administration set is a singl
- Z-0958-2021 · Dec 2, 2020 · Terminated154 cm (61 IN) APPX 1.5ml, PUR YELLOW EXT, 1.2 MICRON FILTER - Product Usage: The intravascular administration set is a single use, sterile, non pyrogenic device, which provides ac
- Z-0957-2021 · Dec 2, 2020 · Terminated7 IN (18cm) APPX 0.43ml, SMALLBORE SET, MicroCLAVE, FILTER SetSource - Product Usage: The intravascular administration set is a single use, sterile, non pyrogenic device, which pro
- Z-0955-2021 · Dec 2, 2020 · Terminated60 IN (152cm) APPX 1.5 ml, PUR YELLOW SMALLBORE SET, FILTER REF B2209 - Product Usage: The intravascular administration set is a single use, sterile, non pyrogenic device, which pr
- Z-0227-2021 · Jul 6, 2020 · Terminated142 IN (361cm) APPX 18.8 ml, 15 DROP SET 4 MicroClave CLEAR, REMV 3-PORT NanoClave w/ BCV. 1 unit per pouch, 25 pouches per case. UDI:(01)10887709089393(17)250101(30)25(10)4573948
- Z-0246-2021 · Jul 6, 2020 · Terminated40 (102cm) Appx 4.4ml Ext Set, 4-Way Clave Stopcock, Clave, 2 Clamps, Rotating Luer, 1 Ext. 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709014531(17)250101(30)5
- Z-0240-2021 · Jul 6, 2020 · Terminated11 IN(28cm)APPX 0.97ml,SMALLBORE SET,NanoClave,6-PORT NanoClave MANIFOLD,BCV.1 unit per pouch, 50 pouches per case. UDI:(01)10887709088354(17)250101(30)50(10)4557643. The Intr
- Z-0254-2021 · Jul 6, 2020 · Terminated22" (56 cm) Appx 2.5 ml, Ext Set w/4-Way Clave Stopcock, Clamp, Luer Lock. 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709051967(17)250101(30)50(10)4605591; (01)10
- Z-0219-2021 · Jul 6, 2020 · Terminated113" (287 cm) Appx 14.7 ml, 10 Drop Admin Set w/MicroClave" Clear, Remv 4-Way NanoClave" Stopcock, Remv 2-Gang 4-Way NanoClave" Stopcocks, Spin Luer w/ Filter Cap, 2 Ext.1 unit per
- Z-0216-2021 · Jul 6, 2020 · Terminated54 IN (137 cm) APPX 7.2 ml EXT SET w NanoClave 4-Way Stopcock ;UDI:(01)10840619082526(17)250201(30)50(10)4718579. The Intravascular Administration Set is a single use, sterile,
- Z-0247-2021 · Jul 6, 2020 · Terminated7 IN (18CM) APPX 0.26ml, SMALLBORE EXT SET, MicroClave, Clave T-Connector.1 unit per pouch, 50 pouches per case. UDI: (01)10887709018065(17)250101(30)50(10)4572133. The Intrava
…and 173 more.
Other Stopcock, i.V. Set devices
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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