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ICU Medical MC33563Recalls & reported problems

Icu Medical, Inc. · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887709057838), received between Sep 2, 2022 and Sep 2, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “No Flow” (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

  • No Flow1

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.

  • MalfunctionSep 2, 2022No Flow; No Flow

    THE EVENT OCCURRED ON AN UNSPECIFIED DATE AND INVOLVED A 60" (152 CM) APPX 1.8 ML, SMALLBORE EXT SET W/REMV MICROCLAVE® CLEAR, CLAMP (BLUE), LUER LOCK. THE REPORTER STATED A PATIENT'S MANIFOLD WAS PRIMED IN THE OPERATING ROOM WITH THE SUBSTITUTION TUBING AND THE CLEAR CAPS WERE REMOVED OFF EACH OF THE LINES. THE TUBING IS 1.8 AND BIGGER THAN THE CONTINUOUS TUBING THEY USUALLY USE FOR MANIFOLDS. THE BEDSIDE NURSE STATED THERE WAS BLOOD BACKING UP INTO THE MANIFOLD. AFTER TRYING TO TROUBLE SHOOT THE PUMPS AND INCREASING THE CARRIER TO 5ML/HR TO ATTEMPT TO CLEAR THE LINE, THE NURSE ULTIMATELY HAD TO DISCONNECT THE LINE CLOSEST TO THE PATIENT TO ASSESS IF THE LINE WAS CLOTTED. ONCE SHE DISCONNECTED THE LINE A LOT OF FLUID EXPELLED FROM THE MANIFOLD. THE BEDSIDE NURSE WAS INSTRUCTED TO PUSH THE NORMAL SALINE CARRIER THROUGH THE MANIFOLD TO CLEAR THE BLOOD. AFTER SHE STOPPED PUTTING PRESSURE ON THE BACK OF THE SYRINGE, THE MANIFOLD SUCKED IN AIR. STAFF HAS HAD ISSUES WITH THIS SUBSTITUTE TUBING BACKING UP AIR AFTER PRESSURE IS RELEASED FROM THE BACK OF THE SYRINGE. ULTIMATELY THEY WERE ABLE TO CLEAR THE MANIFOLD AND LINE WITH CONTINUOUS PRESSURE ON ALL OF THE SYRINGES. THE PATIENT WAS ON

    Patient problems: Low Blood Pressure/ Hypotension

    MAUDE report 15348387 ↗

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-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-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-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-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-0235-2021 · Jul 6, 2020 · Terminated
    10 IN (25cm) APPX 1.5ml EXT w/6-Port NanoClave Manifold, Check Valve. 1 unit per pouch, 50 pouches per case. UDI:(01)10887709067322(17)250101(30)50(10)4565730; (01)10887709067322(
  • Z-0207-2021 · Jul 6, 2020 · Terminated
    13 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-0227-2021 · Jul 6, 2020 · Terminated
    142 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-0244-2021 · Jul 6, 2020 · Terminated
    128" (325 cm) Appx 16.6 ml, 15 Drop Primary Set w/2 MicroClave, Remv 2 Gang 4-Way Clave Stopcock, Rotating Luer, 2 Ext. 1 unit per pouch, 50 multivac pouches per case.UDI:(01)10887
  • Z-0217-2021 · Jul 6, 2020 · Terminated
    Appx 0.82 ml, 3 Gang 4-Way NanoClave Stopcock w/Baseplate, Rotating Luer; 1 unit per pouch, 50 multivac pouches per case. UDI:(01)10887709084435(17)250101(30)50(10)
  • 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-0243-2021 · Jul 6, 2020 · Terminated
    78" (198 cm) APPX 1.7ml, EXT SET, MicroClave Clear, 6-PORT NanoClave MANIFOLD, FILTER .1 unit per pouch, 50 pouches per case. UDI:(01)10887709121703(17)250201(30)50(10)4723226.

…and 173 more.

Other Stopcock, i.V. Set devices

All Stopcock, i.V. Set devices →

Sources and updates

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