ICU Medical Z3535Recalls & reported problems
Icu Medical, Inc. · 7" Smallbore Trifuse Ext Set w/3 MicroClave® Clear, 3 Clamps, Luer Lock · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887709033207), received between Mar 31, 2023 and Mar 31, 2023 — classified as 1 injury.
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.
Most reported problems
Device problems
- Fluid/Blood Leak1
- Retraction Problem1
Patient problems
- Low Blood Pressure/ Hypotension1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 31, 2023Fluid/Blood Leak; Retraction Problem; Fluid/Blood Leak; Retraction Problem
THE EVENT INVOLVED A 7" SMALLBORE TRIFUSE EXT SET W/3 MICROCLAVE® CLEAR, 3 CLAMPS, LUER LOCK, WHERE IT WAS REPORTED THAT THE RUBBER PIECE OF CLAVE REMAINED PUSHED DOWN AND DID NOT RETRACT WHEN REMOVING MEDICATION FROM LINE. THIS RESULTED IN VASOPRESSORS LEAKING OUT OF THE CLAVE AND NOT REACHING A CRITICALLY ILL PATIENT, REQUIRING MULTIPLE MEDICATIONS FOR HEMODYNAMIC STABILITY. THE PATIENT HAD A DRASTIC ABRUPT DROP IN BLOOD PRESSURE REQUIRING SWIFT MEDICAL INTERVENTIONS FOR HEMODYNAMIC SUPPORT AND STABILITY.
Patient problems: Low Blood Pressure/ Hypotension
MAUDE report 16655112 ↗
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: 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-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-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-0228-2021 · Jul 6, 2020 · Terminated112 IN (284cm) APPX 14.8ml, 15 Drop Set 3 MicroClave, Remv 3-Port NanoClave Manifold, BCV.1 unit per pouch, 25 pouches per case. UDI:(01)10887709089904(17)250101(30)25(10)4713954.
- Z-0207-2021 · Jul 6, 2020 · Terminated13 IN(33cm) APPX 1.0 ml, SMALLBORE SET, 4 MicroClave Clear, NanoClave T-Conn, Filter; 1 unit per pouch, 50 pouches per case. UDI:(01)10887709085210(17)250101(30)50(10)4572801; (01)
- 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, n
- Z-0215-2021 · Jul 6, 2020 · Terminated29 IN (74 cm) APPX 3.9 ml, EXT SET w/ NanoClave 4-Way Stopcock; 1 unit per pouch, 50 pouches per case. UDI:(01)10840619082533(17)250101(30)50(10)4605138. The Intravascular Admi
- Z-0262-2021 · Jul 6, 2020 · Terminated8 IN (20CM) APPX 1.3ml, EXT SET w/3-Port NanoClave Manifold, Check Valve.1 unit per pouch, 50 pouches per case. UDI:(01)10887709085814(17)250101(30)50(10)4605676. CLAVE Neutron i
- Z-0230-2021 · Jul 6, 2020 · Terminated114" (290 cm) 60 Drop 150ml Burette Set (Clave, Shut Off, Filter) w/4 Clave Remv 3-Port NanoClave Manifold, 2 Check Valves, Rotating Luer, 2 Exts. 1 unit per pouch, 25 pouches per
- Z-0225-2021 · Jul 6, 2020 · Terminated112 IN (284cm) APPX 14.7ml 15 DROP SET 2 MicroClave, Remv 3-Port NanoClave Manifold, BCV.1 unit per pouch, 25 pouches per case. UDI:(01)10887709088501(17)250201(30)25(10)4733705.
…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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