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ICU Medical B33150Recalls & reported problems

Icu Medical, Inc. · 7" (18 cm) Appx 0.24 ml, Smallbore Pressure Infusion (400psig) Ext Set w/MicroClave®, Purple Clamp, Rotating Luer · 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 00887709006522), received between Jan 15, 2020 and Jan 15, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Puncture/Hole” (1 report).

8 other recalls cover devices cleared under the same FDA submission (K100576); 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

  • Material Puncture/Hole1

Patient problems

  • Exposure to Body Fluids1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 15, 2020Material Puncture/Hole

    UPON FLUSHING POWERGLIDE MIDLINE, EXTENSION SET DEVICE WAS FOUND TO HAVE HOLE OR SPLIT ON CATHETER JUST BELOW HUB, FLUID SQUIRTED OUT AT NURSE'S FACE. THE DEVICE WAS IMMEDIATELY REMOVED FROM THE PATIENT. NURSE FLUSHING THE CATHETER HAD FACIAL EXPOSURE TO BLOOD DUE TO FAULTY CATHETER. MASK WAS COVERING NOSE AND FACE, BUT UNSURE IF EYES WERE EXPOSED. LABS WERE DRAWN OF PATIENT WHO CATHETER WAS IN. POST EXPOSURE PROPHYLAXIS WAS NOT INDICATED. MANUFACTURER RESPONSE FOR SET, ADMINISTRATION, INTRAVASCULAR, ICU MEDICAL (PER SITE REPORTER). MANUFACTURER WILL BE MADE AWARE AND DEVICE RETURNED TO VENDOR FOR QA.

    Patient problems: Exposure to Body Fluids

    MAUDE report 9590712 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K100576. One submission often covers many models, so check the product and lot details in each record.

  • Z-3160-2026 · May 12, 2026 · Open, Classified
    IV Sets with drip chambers
  • Z-1720-2022 · Aug 1, 2022 · Open, Classified
    8.5" (22 cm) Appx 0.85 ml, Bifuse Pressure Infusion (400 psig) Ext Set w/2 Remv MicroClave Clear, 2 Purple Clamps, Rotating Luer;
  • Z-0197-2021 · Jul 6, 2020 · Terminated
    7" (18 cm) Appx 0.31 ml, Smallbore Pressure Infusion (400psig) Ext Set w/Remv MicroClave Clear, Clamp, NanoClave T-Connector (Purple Ring), Rotating Luer; unit per pouch, 50 multi
  • Z-0192-2021 · Jul 6, 2020 · Terminated
    9.5" (24 cm) Appx 0.45 ml, Smallbore Pressure Infusion (400 psig) Ext Set w/MicroClave, 2 NanoClave, NanoClave T-Connector, 3 Purple Clamps, Rotating Luer. 1 unit per pouch, 50 mul
  • Z-0193-2021 · Jul 6, 2020 · Terminated
    6.5" (17 cm) Appx 0.30 ml, Smallbore Pressure Infusion (400psig) Ext Set w/Remv MicroClave, NanoClave T-Connector, Purple Clamp, Rotating Luer. 1 unit per pouch, 50 multivac pouche
  • Z-0204-2021 · Jul 6, 2020 · Terminated
    6.5" (17 cm) Appx 0.35 ml, Smallbore Pressure Infusion (400 psig) Ext Set w/Remv MicroClave Clear, NanoClave, Purple Clamp, Rotating Luer; 1 unit per pouch, 50 multivac pouches per
  • Z-0201-2021 · Jul 6, 2020 · Terminated
    7" (18 cm) Appx 0.32 ml, Smallbore Pressure Infusion (400 psig) Ext Set w/Remv MicroClave Clear, NanoClave, Purple Clamp, Luer Lock; 1 unit per pouch, 50 multivac pouches per case.
  • Z-1916-2020 · Oct 4, 2019 · Terminated
    REF: Z2560, 100" 10 Drop Admin Set w/Hand Pump, 2 Clave", Rotating Luer, 1 Pressure Infusion (400psig) Ext, Purple Clamp, UDI: (01)(01)00887709026889

Other Set, administration, intravascular devices

All Set, administration, intravascular devices →

Sources and updates

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