CP5Recalls & 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
- 96
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls
- 1
We found 4 models of CP5 by LivaNova Deutschland GmbH in the FDA's device registry (GUDID). Together they are named in 96 adverse event reports in the FDA's MAUDE database, received between Nov 30, 2016 and Sep 16, 2026 — classified as 3 injuries, 93 malfunctions.
The most frequently reported specific device problem is “Pumping Stopped” (38 reports).
1 FDA recall record name at least one of these models by its device identifier.
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
CP5 recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Oct 30, 2017Terminated
Possibility that the automatic line closure by the Electronic Remote-Controlled (ERC) clamp after detection of an air bubble could take longer than is intended by design in the CP5 system.
Z-0401-2018 · Root cause: Device Design · names 3 of these models · Recall details · FDA record ↗
Most reported CP5 problems
Device problems
- Pumping Stopped38
- No Display/Image12
- Pumping Problem9
- Infusion or Flow Problem6
- Device Displays Incorrect Message5
- Unexpected Shutdown4
- Decreased Pump Speed3
- Insufficient Flow or Under Infusion3
Patient problems
- No Clinical Signs, Symptoms or Conditions63
- No Consequences Or Impact To Patient24
- No Patient Involvement9
CP5 models
4 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CP5 Pump Control PanelControl, pump speed, cardiopulmonary bypass1 recall53 reports
- CP5 Drive UnitControl, pump speed, cardiopulmonary bypass1 recall32 reports
- CP5 Emergency SystemControl, pump speed, cardiopulmonary bypass1 recall2 reports
- CP5 Pump Control PanelControl, pump speed, cardiopulmonary bypass9 reports
Recent CP5 adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 16, 2026Complete Loss of Power
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50783874 ↗MalfunctionApr 17, 2026Pumping Stopped
LIVANOVA RECEIVED A REPORT ABOUT A CP5 SYSTEM DISPLAYING THE ERROR MESSAGE "MOTOR CONTROL FAILURE". THE EVENT OCCURRED DURING PRIMING. THERE IS NO REPORT OF ANY PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24911192 ↗MalfunctionMar 11, 2026Pumping Problem
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT THE CENTRIFUGAL PUMP CP5, USED AS ARTERIAL PUMP, PROVIDED UNSTABLE FLOW DURING PROCEDURE. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24573777 ↗MalfunctionDec 24, 2025Pumping Problem; Pumping Problem
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23886736 ↗MalfunctionOct 17, 2025Pumping Stopped; Pumping Stopped
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23325841 ↗MalfunctionAug 7, 2025Pumping Stopped; Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT, POST-PROCEDURE, THE CP5 GAVE SHORT INTERNAL ERROR MESSAGE (NO CODE). THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22735676 ↗MalfunctionJun 12, 2025Pumping Stopped; Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT, JUST BEFORE THE PROCEDURE STARTED, THE CP5 PUMP WAS STOPPED. THIS WAS USED AS A SUCTION. THE PERFUSIONIST WAS THEN ABLE TO QUICKLY SWITCH TO ANOTHER PUMP THAT WAS FREE. THERE IS NO REPORT OF ANY PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22195034 ↗MalfunctionMay 26, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
LIVANOVA DEUTSCHLAND RECEIVED A REPORT OF AN ISSUE WITH CP5 DRIVER UNIT. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22084826 ↗MalfunctionFeb 25, 2025Structural Problem; Structural Problem
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21458348 ↗MalfunctionNov 8, 2024Pumping Problem; Pumping Problem
LIVANOVA RECEIVED A REPORT THAT A YELLOW ICON SHOWED UP WHEN CUSTOMER TRIED TO FORWARD THE FLOW, THE CP5 HAD DROPPED THE FLOW TO 0 AND THERE WAS NO FORWARD FLOW. PERFUSIONIST CANNOT RECALL THE INFORMATION ASSOCIATED TO THE DISPLAYED ALARM (YELLOW TRIANGLE ALARM ON CP5 PANEL). THROUGH FOLLOW UP, THE PERFUSIONIST INFORMED LIVANOVA THE PUMP WOULD NOT HAVE FORWARD FLOW FOR ABOUT 5-7 MINUTES. THERE IS NO REPORT OF ANY PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20637895 ↗MalfunctionNov 6, 2024Pumping Stopped; Pumping Stopped
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20619380 ↗MalfunctionOct 31, 2024Pumping Stopped; Pumping Stopped
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20578109 ↗MalfunctionOct 30, 2024Pumping Stopped; Pumping Stopped
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT A CP5 GAVE AN ERROR MESSAGE AND PUMP DID NOT RUN. THE ISSUE OCCURRED AT SETUP. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20565932 ↗MalfunctionOct 23, 2024Unexpected Shutdown; Unexpected Shutdown
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT THE SCREEN OF A CP5 SHUT OFF DURING PROCEDURE. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20512542 ↗MalfunctionOct 10, 2024Pumping Problem; Pumping Problem
SEE INITIAL REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20415955 ↗
Other LivaNova Deutschland GmbH products
- Heater-Cooler System2 models · 311 reports · 1 recall
- ESSENZ8 models · 185 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
- 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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