ICU Medical MC330209Recalls & reported problems
Icu Medical, Inc. · 6" (15 cm) Appx 0.90 ml, Smallbore Trifuse Ext Set w/3 MicroClave™ Clear, 0.2 Micron Filter, 1.2 Micron Filter, 3 Clamps (Blue, Yellow, White), Rotating Luer · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887709080546), received between Oct 5, 2020 and Oct 5, 2020 — classified as 1 death.
The most frequently reported specific device problem is “Failure to Infuse” (1 report).
1 FDA recall record name this device's identifier.
187 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.
Recalls naming this device
- Jul 1, 2020Class IITerminated
Incorrect filter assemblies in IV administration set.
Z-0511-2021 · Root cause: Component design/selection · Recall details · FDA record ↗
Most reported problems
Device problems
- Failure to Infuse1
Patient problems
- Death1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
DeathOct 5, 2020Failure to Infuse; Failure to Infuse
THE EVENT INVOLVED A 6" (15 CM) APPX 0.90 ML, SMALLBORE TRIFUSE EXT SET W/3 MICROCLAVE® CLEAR, 0.2 MICRON FILTER, 1.2 MICRON FILTER, 3 CLAMPS (BLUE, YELLOW, WHITE), ROTATING LUER, THAT DURING INFUSION, THE 1.2 MICRON FILTER INFUSING LIPIDS CLOGGED, ALLOWING NO FLUID TO GO THROUGH IT. TOTAL PARENTERAL NUTRITION (TPN) WAS BEING INFUSED VIA THE 0.2 MICRON FILTER OF THE DEVICE. THE TUBING SET HAD BEEN IN USE FOR LESS THAN 24 HOURS. THE SET-UP OF THE DEVICE WAS A SYRINGE CONTAINING LIPIDS WITH AN EXTENSION SET ATTACHED TO THE 1.2 MICRON FILTER (PART OF THE TRI-FUSE) THAT CLOGGED. IT WAS REPORTED THAT THE TRI-FUSE EXTENSION SET CONTAINING THE CLOGGED FILTER WAS REPLACED. IT WAS REPORTED THAT THE PATIENT, A BABY, HAS DIED, BUT NOT AS A RESULT OF THE FILTER BEING CLOGGED. THE BABY BECAME ACIDOTIC AS A RESULT OF DEHYDRATION. THE DATE OF DEATH IS UNKNOWN.
Patient problems: Death
MAUDE report 10631293 ↗
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-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-0242-2021 · Jul 6, 2020 · Terminated11 IN (28cm) APPX 1.5ml EXT SET NanoClave, 6-Port NanoClave Manifold . 1 unit per pouch, 50 pouches per case. UDI:(01)10887709098937(17)241201(30)50(10)4493669;(01)10887709098937(
- Z-0184-2021 · Jul 6, 2020 · Terminated6" (15 cm) Appx 0.24 ml, Smallbore Ext Set w/MicroClave Clear, Clamp, NanoClave T-Connector, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case; UDI: (01)10887709051031(
- Z-0195-2021 · Jul 6, 2020 · Terminated109" (277 cm) Appx 8.6 ml, Transfer Set w/Check Valve, NanoClave T-Connector, Anti-Siphon Valve, 4 Clamps, Smallbore Trifuse Ext Set w/2 MicroClave Clear, 0.2 Micron Filter, Rotati
- Z-0249-2021 · Jul 6, 2020 · Terminated6 IN (15 cm) Ext Set, MicroClave Clear, T-Connector, RLL, Approx PV: 0.86 mL.1 unit per pouch, 50 pouches per case. UDI:(01)10887709079877(17)250101(30)50(10)4584753;(01)108877090
- Z-0185-2021 · Jul 6, 2020 · Terminated5 IN(13cm) APPX 0.87ml, EXT SET,NanoClave T-CONNECTOR; 1 unit per pouch, 50 pouches per case; UDI: (01)10887709052809(17)250101(30)50(10)4599980.
- Z-0241-2021 · Jul 6, 2020 · Terminated6 IN (15cm) APPX 0.89ml, Smallbore Set 6-Port NanoClave Manifold.1 unit per pouch, 50 pouches per case. UDI:(01)10887709087719(17)250101(30)50(10)4558621;(01)10887709087719(17)2501
- Z-0251-2021 · Jul 6, 2020 · Terminated60 IN (152cm) APPX 1.1ml, TRIFUSE, Clave STOPCOCK, 2 Clave, FILTER. 1 unit per pouch, 50 pouches per case. UDI:(01)10887709040103(17)250201(30)50(10)4726780. The Intravascular Ad
…and 172 more.
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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 · each recall links to the FDA recall notice
- 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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