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, ClassifiedHotline 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 · TerminatedSmiths 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 · TerminatedSmiths 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 · TerminatedSmiths 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 · TerminatedLevel 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 · TerminatedHOTLlNE 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 · TerminatedHOTLlNE 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 · TerminatedHOTLlNE 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 · TerminatedHOTLlNE 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 · TerminatedLevel 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 · TerminatedHOTLlNE 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
- Level 1 HL-90Icu Medical, Inc. · Warmer, thermal, infusion fluid991 reports
- Level 1 HL-390Icu Medical, Inc. · Warmer, thermal, infusion fluid634 reports
- Level 1 L-70Icu Medical, Inc. · Warmer, thermal, infusion fluid1 recall385 reports
- 3-Spike Disposable Set (1 Piece) 903-00006PBelmont Instrument Corporation · Warmer, Thermal, Infusion Fluid1 recall1 death97 reports
- Rapid Infuser RI-2, 120V, 750 ml/min 903-00039Belmont Instrument Corporation · Warmer, Thermal, Infusion Fluid132 reports
- Level 1 L-70NIIcu Medical, Inc. · Warmer, thermal, infusion fluid114 reports
- Rapid Infuser RI-2, 120V, 1000ml/min 903-00037Belmont Instrument Corporation · Warmer, Thermal, Infusion Fluid1 death76 reports
- Hyperthermia Pump Procedure Kit 902-00045Belmont Instrument Corporation · Warmer, Thermal, Infusion Fluid1 recall4 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.