ICU Medical 011-C3322Recalls & reported problems
Icu Medical, Inc. · 5" (13 cm) Appx 0.33 ml, Smallbore Bifuse Ext Set w/2 MicroClave™, 2 Clamps, Rotating Luer · Class 2
Data updated Oct 18, 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 00840619001742), received between Sep 15, 2022 and Aug 23, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (1 report).
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak1
- Separation Problem1
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.
MalfunctionAug 23, 2024Separation Problem; Separation Problem
THE EVENT OCCURRED ON AN UNSPECIFIED DATE AND INVOLVED A 13 CM (5") APPX 0.33 ML, SMALLBORE BIFUSE EXT SET W/2 MICROCLAVE¿, ROTATING LUER LOCK WHERE IT WAS REPORTED THE "PARTS SEPERATED AND FELL OFF" RESULTING IN BLEED BACK. THIS CAUSES AN EMBOLISM RISK AND INFECTION RISK TO THE PATIENT DUE TO THE LINES ATTACHED TO SIT IN THE PATIENT¿S HEART. THERE WAS PATIENT INVOLVEMENT AND UNKNOWN HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20048741 ↗MalfunctionSep 15, 2022Fluid/Blood Leak; Fluid/Blood Leak
THE EVENT INVOLVED A 5" (13 CM) APPX 0.33 ML, SMALLBORE BIFUSE EXT SET W/2 MICROCLAVE®, 2 CLAMPS, ROTATING LUER. THE CUSTOMER REPORTED THAT THERE WAS LEAKAGE OF CHEMOTHERAPY MEDICATION ON THE UNUSED PART OF THE BIFUSE CONNECTOR. THE BIFUSE (WITH 2 CLAVE) WAS USED AS CONNECTED TO THE PATIENT¿S IV LINE SINCE THE PATIENT WOULD HAVE AN ESSAY PUMP CHEMOTHERAPY INFUSION THAT WOULD BE BROUGHT TO THE PATIENT'S HOME. THE PATIENT WAS DISCHARGED SUBSEQUENTLY THAT DAY AFTER HIS IV LINE WAS CHECKED THOROUGHLY AND CAREFULLY FOR PATENCY AND LEAKS. LATER THAT DAY, THE PATIENT WENT BACK TO THE HOSPITAL AFTER OBSERVING THE MEDICATION LEAKAGE. THE HOSPITAL¿S EMERGENCY DEPARTMENT MANAGED THE MEDICATION LEAKAGE INCIDENT THEREAFTER. THE EVENT OCCURRED DURING THE PROCEDURE/INFUSION. THERE WAS PATIENT INVOLVEMENT AND NO HUMAN HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15428515 ↗
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-3157-2026 · May 12, 2026 · Open, ClassifiedIV Non-Dedicated Gravity Administration Sets with drip chambers
- Z-3163-2026 · May 12, 2026 · Open, ClassifiedIV 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: B
- 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-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-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-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-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-0202-2021 · Jul 6, 2020 · Terminated8" (20 cm) Appx 0.53 ml, Smallbore Ext Set w/MicroClave Clear, 0.2 Micron Filter, NanoClave T-Connector, Clamp, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case. UDI:(
- Z-0196-2021 · Jul 6, 2020 · Terminated7.5" (19 cm) Appx 0.59 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear (Yellow, Green, Purple Rings), NanoClave T-Connector, 4 Clamps, Rotating Luer. UDI:(01)10887709067049(17)2
- Z-0211-2021 · Jul 6, 2020 · Terminated5.5" (14 cm) Appx 0.50 ml, Smallbore Trifuse Ext Set w/3 MicroClave" Clear, NanoClave" T-Connector, 3 Clamps, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case.UDI:(01)
- Z-0229-2021 · Jul 6, 2020 · Terminated78 IN (198cm) APPX 10.0 ml, 20 Drop Set 3-Port NanoClave Manifold, BCV, MicroClave. 1 unit per pouch, 24 pouches per case.UDI:(01)10887709090634(17)241201(30)25(10)4537328. The I
- Z-0218-2021 · Jul 6, 2020 · Terminated126" (320 cm) 16.4 ml, 15 Drop Primary Set w/2 MicroClave Clear, Remv 2 Gang 4-Way NanoClave Stopcock, Rotating Luer, 1 Ext; 1 unit per pouch, 50 multivac pouches per case. UDI:(01
- Z-0210-2021 · Jul 6, 2020 · Terminated13 IN (33cm) APPX 0.96 ml, PENTAFUSE SMALLBORE SET, NanoClave, 3 MicroClave Clear. 1 unit per pouch, 50 pouches per case. UDI:(01)10887709090245(17)250101(30)50(10)4557533; (01)108
- Z-0191-2021 · Jul 6, 2020 · Terminated5" (13 cm) Appx 0.39 ml, Smallbore Bifuse Ext Set w/NanoClave T-Connector, 2 Clamps, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709053028(17)250101
…and 173 more.
Other Stopcock, i.V. Set devices
- Connecta, Luer-Lok 394910BD Switzerland Sàrl · Stopcock, i.V. Set3 recalls8 reports
- Outlook® 490361B. Braun Medical Inc. · Stopcock, i.V. Set3 recalls0 reports
- Blood Administration Set 490530B. Braun Medical Inc. · Stopcock, i.V. Set2 recalls11 reports
- Medex MX9341LIcu Medical, Inc. · Stopcock, i.V. Set63 reports
- ICU Medical AC135Icu Medical, Inc. · Stopcock, i.V. Set1 recall10 reports
- IV Administration Set 490067B. Braun Medical Inc. · Stopcock, i.V. Set1 recall9 reports
- ICU Medical MC330174Icu Medical, Inc. · Stopcock, i.V. Set1 recall4 reports
- ICU Medical Z2587Icu Medical, Inc. · Stopcock, i.V. Set1 recall3 reports
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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