S5 Mast Roller PumpRecalls & reported problems across all models
LivaNova Deutschland GmbH · 4 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 47
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls
- 0
We found 4 models of S5 Mast Roller Pump by LivaNova Deutschland GmbH in the FDA's device registry (GUDID). Together they are named in 47 adverse event reports in the FDA's MAUDE database, received between Jul 19, 2016 and Aug 25, 2026 — classified as 1 injury, 46 malfunctions.
The most frequently reported specific device problem is “Pumping Stopped” (31 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 Mast Roller Pump problems
Device problems
- Pumping Stopped31
- No Display/Image4
- Pumping Problem4
- Appropriate Device Problem Term/Code Not Available2
- Insufficient Device Problem Information2
- Decreased Pump Speed1
- Display or Visual Feedback Problem1
- Failure to Auto Stop1
Patient problems
- No Clinical Signs, Symptoms or Conditions34
- No Consequences Or Impact To Patient7
- No Patient Involvement5
- Brain Injury1
S5 Mast Roller Pump models
4 models, most reported first. Each model has its own page with its reports, recalls and device details.
- S5 Mast Roller Pump MRP 150CONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS23 reports
- S5 Mast Roller Pump MRP 85CONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS12 reports
- S5 Mast Roller Pump Control Panel for 1 MRPCONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS11 reports
- S5 Mast Roller Pump Control Panel for 2 MRP85CONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS1 report
Recent S5 Mast Roller Pump adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionAug 25, 2026Pumping Stopped
LivaNova Deutschland received a report of an S5 Mast Roller Pump 85 for which a motor controller error occurred (432, "Fault in motor controller"). There was no patient injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50428663 ↗MalfunctionMar 30, 2026Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT THE PUMP HEAD OF AN S5 MAST ROLLER PUMP 150 WAS NOT ROTATING SMOOTHLY AND WAS FREQUENTLY GIVING MESSAGE "MAXIMUM LOAD LIMIT IS REACHED" DURING PRIMING. THERE WAS NO PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24710692 ↗MalfunctionAug 8, 2025Pumping Stopped; Pumping Stopped
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22751628 ↗MalfunctionJul 1, 2025Pumping Problem; Pumping Problem
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22372431 ↗MalfunctionMar 14, 2025Pumping Stopped; Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT, DURING PRIMING, CARDIOPLEGIA S5 MAST ROLLER PUMP STOPPED RUNNING. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21604246 ↗MalfunctionOct 16, 2024Pumping Stopped; Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT AN S5 PUMP GAVE A MOTOR CONTROLLER ERROR MESSAGE DURING BYPASS. CUSTOMER WAS NOT ABLE TO TURN THE PUMP VIA THE DIAL, NO REVOLUTIONS POSSIBLE. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20459259 ↗MalfunctionOct 11, 2024Pumping Stopped; Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT, WHEN SWITCHING ON THE S5 SYSTEM, MASTER PUMP ALARM FAULT IN THE MOTOR CONTROL (429). THERE IS NO REPORT OF ANY PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20426232 ↗MalfunctionOct 10, 2024Pumping Stopped; Pumping Stopped
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20415953 ↗MalfunctionJul 22, 2024Failure to Auto Stop; Failure to Auto Stop
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT ARTERIAL PUMP DID NOT STOP, DESPITE BEING SELECTED AS CONTROLLED PUMP, WHEN HIGH ARTERIAL PRESSURE ALARM WAS CREATED. NO ADDITIONAL INFORMATION WAS RECEIVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19790300 ↗MalfunctionJul 9, 2024Pumping Stopped; Pumping Stopped
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19701189 ↗MalfunctionJul 9, 2024Pumping Stopped; Pumping Stopped
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19699276 ↗MalfunctionMay 30, 2024Pumping Stopped; Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT, BEFORE STARTING CARDIOPULMONARY BYPASS, THE MAST ROLLER PUMP 85 LOST POWER, THEN RECOVERED NATURALLY, AND THEN AGAIN THE POWER WENT DOWN. BY REPLACING THE TUBING FROM THE DEFECTIVE PUMP TO ANOTHER PUMP, MEDICAL TEAM WAS ABLE TO START CARDIOPULMONARY BYPASS WITHOUT ANY PROBLEMS AND WITHOUT ANY IMPACT ON THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19423623 ↗MalfunctionMay 28, 2024Pumping Stopped; Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT A S5 MAST ROLLER PUMP GAVE A MOTOR CONTROLLER FAILURE ERROR MESSAGE DURING PRIMING. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19403891 ↗MalfunctionApr 10, 2024Pumping Stopped; Pumping Stopped
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19077499 ↗MalfunctionMar 22, 2024Pumping Stopped; Pumping Stopped
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18957688 ↗
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
- S5 Roller Pump 1502 models · 135 reports
- Electronic Gas Blender3 models · 106 reports
- Electrical Remote-Controlled Tubing Clamp3 models · 85 reports
- S5 Double Roller Pump 852 models · 59 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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