S5 Roller Pump 150Recalls & reported problems across all models
LivaNova Deutschland GmbH · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 135
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls
- 0
We found 2 models of S5 Roller Pump 150 by LivaNova Deutschland GmbH in the FDA's device registry (GUDID). Together they are named in 135 adverse event reports in the FDA's MAUDE database, received between Jul 26, 2016 and Feb 20, 2026 — classified as 1 death, 128 malfunctions.
The most frequently reported specific device problem is “Pumping Stopped” (67 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported S5 Roller Pump 150 problems
Device problems
- Pumping Stopped67
- Device Displays Incorrect Message22
- Failure to Power Up13
- No Display/Image13
- Pumping Problem11
- Failure to Auto Stop4
- Appropriate Device Problem Term/Code Not Available3
- Failure to Pump3
Patient problems
- No Clinical Signs, Symptoms or Conditions72
- No Patient Involvement37
- No Consequences Or Impact To Patient23
- Brain Injury1
- Cerebral Edema1
- Insufficient Information1
- Loss of consciousness1
- Low Blood Pressure/ Hypotension1
S5 Roller Pump 150 models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- S5 Roller Pump 150 RP 150CONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS1 death120 reports
- S5 Roller Pump 150 RP 150CONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS15 reports
Recent S5 Roller Pump 150 adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionFeb 20, 2026Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT STATING THAT AN S5 HLM ROLLER PUMP 150 STOPPED RUNNING AFTER THE PROCEDURE. THE INVOLVED PUMP WAS USED AS AN AUXILIARY SUCTION PUMP. THERE IS NO REPORT OF ANY PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24400592 ↗MalfunctionFeb 20, 2026Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT STATING THAT AN S5 HLM ROLLER PUMP 150 STOPPED RUNNING AND ITS DISPLAY WENT BLACK DURING THE PROCEDURE. THE INVOLVED PUMP WAS USED AS AN AUXILIARY SUCTION PUMP. THERE IS NO REPORT OF ANY PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24399207 ↗MalfunctionJan 27, 2026Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT THE S5 HLM SHOWED THE ERROR MESSAGE MOTOR CONTROL FAILURE, RELATED TO ROLLER PUMP 1. THE ISSUE OCCURRED DURING PROCEDURE. THERE IS NO REPORT OF ANY PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24186655 ↗MalfunctionDec 10, 2025Pumping Stopped; Pumping Stopped
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23767847 ↗MalfunctionOct 17, 2025Pumping Stopped; Appropriate Device Problem Term/Code Not Available; Pumping Stopped; Appropriate Device Problem Term/Code Not Available
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT, THE S5 SINGLE ROLLER PUMP 150 DISPLAYED ERROR MOTOR CONTROL FAILURE (E441) AND THE SCREEN TEMPORARILY BECAME BLACK. THE ISSUE OCCURRED DURING PROCEDURE. THERE IS NO REPORT OF ANY PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23325595 ↗MalfunctionSep 19, 2025Pumping Stopped; Pumping Stopped
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23097948 ↗MalfunctionSep 2, 2025Pumping Stopped; Pumping Stopped
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22931807 ↗MalfunctionAug 8, 2025Pumping Stopped; Pumping Stopped
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22747201 ↗MalfunctionJul 21, 2025Pumping Problem; Pumping Problem
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22561452 ↗MalfunctionJun 4, 2025Pumping Stopped; Pumping Stopped
LIVANOVA RECEIVED REPORT THAT THE S5 ROLLER PUMP ALARMED MOTOR OVERSPEED, THEN SHOWED A FAULT IN THE MOTOR CONTROLLER (429), CAUSING THE PUMP HEAD TO STOP WORKING DURING USE, THERE WAS NO REPORT OF PATIENT INJURY
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22139194 ↗MalfunctionMay 31, 2025Pumping Stopped; Pumping Stopped
SEE INTIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22120448 ↗MalfunctionApr 3, 2025Intermittent Loss of Power; Intermittent Loss of Power
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT, DURING A PROCEDURE, THE S5 ROLLER PUMP 150 HAD INTERMITTENT POWER ISSUE. THERE IS NO REPORT OF ANY PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21762428 ↗MalfunctionFeb 20, 2025Pumping Stopped; Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT A S5 ROLLER PUMP 150 GAVE A RUNAWAY ERROR MESSAGE ("THE PUMP RAN TOO FAST: SET VALUE DIFFERENT TO ACTUAL VALUE") AND STOPPED WORKING. THE ISSUE OCCURRED DURING PROCEDURE. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21419256 ↗MalfunctionFeb 6, 2025Pumping Stopped; Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT A S5 ROLLER PUMP 150 DISPLAYED A MOTOR CONTROL ERROR DURING A PROCEDURE. THERE IS NO REPORT OF ANY PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21322630 ↗MalfunctionDec 27, 2024Pumping Problem; Pumping Problem
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21027764 ↗
Other LivaNova Deutschland GmbH products
- Heater-Cooler System2 models · 311 reports · 1 recall
- ESSENZ8 models · 185 reports · 1 recall
- CP54 models · 96 reports · 1 recall
- S5 Console7 models · 141 reports
- Electronic Gas Blender3 models · 106 reports
- Electrical Remote-Controlled Tubing Clamp3 models · 85 reports
- S5 Double Roller Pump 852 models · 59 reports
- S5 Mast Roller Pump4 models · 47 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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