ICU Medical 011-MC3302Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00840619043223), received between Feb 11, 2019 and Jun 27, 2025 — classified as 1 injury, 1 malfunction.

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 27, 2025Unsealed Device Packaging; Unsealed Device Packaging

  A THE EVENT INVOLVED A 7" (18CM) APPX 0.25 ML, SMALLBORE EXT SET W/MICROCLAVE® CLEAR, CLAMP, ROTATING LUER. IT WAS STATED IN THE EMERGENCY OPERATING ROOM OF THIS HOSPITAL, WHERE THEY HAD BEGUN USING THIS ITEM, THEY WERE CONCERNED ABOUT WHETHER IT TRULY CAME STERILE IN ITS PACKAGING. WHEN THEY PRESSED THE PACKAGE, THE PLASTIC COMPRESSED AND, AFTER A WHILE, IT SWELLED UP AGAIN AS IF AIR WAS RE-ENTERING. THEY SUSPECTED THERE MAY BE A HOLE THAT ALLOWED AIR TO ENTER AND EXIT, WHICH LED THEM TO DOUBT ITS STERILITY. THIS CONCERN HAS BEEN FORWARDED TO THE MATERIALS MANAGEMENT DEPARTMENT, WHICH WAS THE ONE WHO RAISED THIS QUESTION OR INCIDENT. THE SAME ISSUE OCCURRED WITH ALL THE LOTS THEY HAVE RECEIVED, WHICH IS WHY THEY ARE QUESTIONING THE STERILITY OF ITEM 011-MC3302. THE STATUS OF THE PRODUCT AT THE TIME OF EVENT WAS UPON REMOVAL OF THE PRIMARY PACKAGE. THE DEVICE WAS NOT REPROCESSED OR RE-STERILIZED. THE EVENT DID NOT OCCUR DURING PATIENT USE, AND RESULTED IN NO DELAY OR ADVERSE EVENT/HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22349468 ↗
• InjuryFeb 11, 2019Fluid/Blood Leak; Fluid/Blood Leak

  THE CUSTOMER CONTACT REPORTED THE EXTENSION SET LEAKED AT THE LEVEL OF THE VALVE, WHILE CONNECTED TO A 5-WAY EXTENSION SET, DURING AN INFUSION OF CAFFEINE. THERE WAS A PEDIATRIC PATIENT INVOLVED AND AN UNSPECIFIED ADVERSE EVENT. NO FURTHER INFORMATION WAS PROVIDED

  Patient problems: Injury

  MAUDE report 8327889 ↗

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, Classified
  IV Non-Dedicated Gravity Administration Sets with drip chambers
• Z-3163-2026 · May 12, 2026 · Open, Classified
  IV Sets with drip chambers
• Z-0154-2026 · Oct 2, 2025 · Open, Classified
  IV 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, Classified
  6.5" (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 · Terminated
  60 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 · Terminated
  7 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-0956-2021 · Dec 2, 2020 · Terminated
  60" (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 · Terminated
  154 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-0242-2021 · Jul 6, 2020 · Terminated
  11 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-0258-2021 · Jul 6, 2020 · Terminated
  112" (284 cm) 60 Drop 150ml Burette Set (Clave, Shut-Off) w/2 MicroClave, Remv 3 Gang 4-Way Clave Stopcock, Check Valve, Rotating Luer, 1 Ext. 1 unit per pouch, 25 pouches per case
• Z-0187-2021 · Jul 6, 2020 · Terminated
  7" (18cm) Appx 0.31 ml, Smallbore Ext Set w/Remv MicroClave Clear, NanoClave T-Connector, Clamp, Rotating Luer. 1 unit per pouch, 50 multivac pouches per case. UDI:(01)108877090510
• Z-0184-2021 · Jul 6, 2020 · Terminated
  6" (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-0226-2021 · Jul 6, 2020 · Terminated
  112 IN(284cm) APPX 14.6ml, 15 Drop Set 3 MicroClave, 3-Port NanoClave Manifold, BCV.1 unit per pouch, 25 pouches per case. UDI:(01)10887709088518(17)241101(30)25(10)4475764 (01)108
• Z-0222-2021 · Jul 6, 2020 · Terminated
  123 IN (312cm) APPX 16.1 ml, 10 DROP SET w/3 MicroClave, 3-Port NanoClave; UDI:(01)10887709085432(17)241201(30)25(10)4536733;(01)10887709085432(17)250101(30)25(10)4573641. The In
• Z-0221-2021 · Jul 6, 2020 · Terminated
  83" (211 cm) Smallbore Ext Set w/Remv 8 Gang 4-Way NanoClave Stopcock w/Baseplate, Rotating Luer;1 unit per pouch, 25 pouches per case. UDI:(01)10887709089508(17)250101(30)25(10)45

…and 173 more.