Skip to content

Level 1 HL-390-40Recalls & reported problems

Icu Medical, Inc. · Class 2

Adverse event reports
3
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10695085002833), received between Oct 13, 2021 and Jul 11, 2023 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Defective Alarm” (1 report).

11 other recalls cover devices cleared under the same FDA submission (K911383); 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Defective Alarm1
  • Device Alarm System1
  • Failure to Deliver1
  • Insufficient Device Problem Information1
  • No Apparent Adverse Event1

Patient problems

  • Insufficient Information2
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 11, 2023Device Alarm System; Defective Alarm; Device Alarm System; Defective Alarm

    IT WAS REPORTED THAT THE ALARMS ARE NOT FUNCTIONING ON THE DEVICE. NO PATIENT INVOLVEMENT WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17302440 ↗
  • MalfunctionFeb 21, 2023Failure to Deliver; Failure to Deliver

    IT WAS REPORTED THAT THE DEVICES DISPOSABLE CASSETTE SENSOR WAS NOT WORKING. THERE HAS BEEN NO REPORT OF PATIENT INVOLVEMENT OR NO OBSERVABLE CLINICAL SYMPTOMS OR A CHANGE IN SYMPTOMS IDENTIFIED IN THE PATIENT.

    Patient problems: Insufficient Information

    MAUDE report 16408501 ↗
  • InjuryOct 13, 2021No Apparent Adverse Event; Insufficient Device Problem Information; No Apparent Adverse Event; Insufficient Device Problem Information

    AN UNKNOWN CUSTOMER ISSUE WAS REPORTED FOR A LIFE-SUSTAINING DEVICE.

    Patient problems: Insufficient Information

    MAUDE report 12628902 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K911383. One submission often covers many models, so check the product and lot details in each record.

  • Z-2759-2026 · Jun 24, 2026 · Open, Classified
    Hotline Fluid Warming Set, single use device, is designed to warm blood and intravenous fluids and deliver them to the patient's intravenous access site at normothermic temperature
  • Z-1444-2014 · Mar 17, 2014 · Terminated
    Smiths Medical HOTLINE Fluid Warming Set L-80. Product Usage: intended for the delivery of warmed blood and intravenous fluids at normothermic temperatures under gravity condit
  • Z-1443-2014 · Mar 17, 2014 · Terminated
    Smiths Medical HOTLINE Fluid Warming Set L-70. Product Usage: intended for the delivery of warmed blood and intravenous fluids at normothermic temperatures under gravity conditio
  • Z-1979-2012 · Jun 27, 2012 · Terminated
    Smiths Medical HOTLINE 3 Blood and Fluid Warmer, Reorder Numbers: HL-390 Product Usage: The Micro-switch is used on the HOTLINE 3 Blood and Fluid Warmer. This product, for use in
  • Z-0428-2012 · Nov 21, 2011 · Terminated
    Level 1 Normothermic I.V. Fluid Administration Sets, Product Code DI-60HL , Product Usage: Single patient use sets designed for use by trained medical professionals, in conjuncti
  • Z-0425-2012 · Nov 21, 2011 · Terminated
    HOTLlNE Disposable Administration Sets, Product Code L-370 Product Usage: Single patient use Sets designed for use by trained medical professionals, in conjunction with HOTLlNE
  • Z-0426-2012 · Nov 21, 2011 · Terminated
    HOTLlNE Disposable Administration Sets, Product Code L-80 Product Usage: Single patient use Sets designed for use by trained medical professionals, in conjunction with HOTLlNE R
  • Z-0423-2012 · Nov 21, 2011 · Terminated
    HOTLlNE Disposable Administration Sets, Product Codes L-70NI Product Usage: Single patient use Sets designed for use by trained medical professionals, in conjunction with HOTLlNE
  • Z-0424-2012 · Nov 21, 2011 · Terminated
    HOTLlNE Disposable Administration Sets, Product Code L-270 Product Usage: Single patient use Sets designed for use by trained medical professionals, in conjunction with HOTLlNE
  • Z-0427-2012 · Nov 21, 2011 · Terminated
    Level 1 Normothermic I.V. Fluid Administration Sets, Product Code D-60HL , Product Usage: Single patient use sets designed for use by trained medical professionals, in conjunctio
  • Z-0422-2012 · Nov 21, 2011 · Terminated
    HOTLlNE Disposable Administration Sets, Product Codes L-70 Product Usage: Single patient use Sets designed for use by trained medical professionals, in conjunction with HOTLlNE R

Other Warmer, thermal, infusion fluid devices

All Warmer, thermal, infusion fluid devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.