E/P Pack S5Recalls & reported problems
LivaNova Deutschland GmbH · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04033817900832), received between Feb 8, 2017 and May 22, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device Displays Incorrect Message” (1 report).
13 other recalls cover devices cleared under the same FDA submission (K071318); 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.
Reports received per month
Most reported problems
Device problems
- Device Displays Incorrect Message1
- No Display/Image1
- Unexpected Shutdown1
Patient problems
- No Patient Involvement2
- 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.
MalfunctionMay 22, 2025Unexpected Shutdown; Unexpected Shutdown
LIVANOVA DEUTSCHLAND RECEIVED A REPORT THAT DURING PROCEDURE ALL ROLLER PUMPS OF A S5 CONSOLE WERE TURNED OFF AND ON BY THEMSELVES. THE PROCEDURE WAS THEN COMPLETED WITHOUT ANY PROBLEMS. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22069798 ↗MalfunctionMar 22, 2017No Display/Image; No Display/Image
LIVANOVA (B)(4) RECEIVED A REPORT THAT THE USER WAS UNABLE TO CHANGE THE PUMP SET-UP OF THE S5 SYSTEM DURING MAINTENANCE. THE SYSTEM WAS POWERED OFF AND BACK ON AND ALL INDICATIONS WERE SHOWN IN ENGLISH AND NOTHING WAS DISPLAYED ON THE SYSTEM PANEL. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Patient Involvement
MAUDE report 6425036 ↗MalfunctionFeb 8, 2017Device Displays Incorrect Message; Device Displays Incorrect Message
SORIN GROUP (B)(4) RECEIVED A REPORT THAT THE S5 E/P PACK DISPLAYED A UPS START-UP ERROR DURING SET-UP. THE CUSTOMER RESTARTED THE UNIT AND THE SAME MESSAGE APPEARED. THE UNIT WAS POWERED OFF FOR A WHILE AND COULD BE STARTED NORMALLY WHEN POWERED BACK ON. HOWEVER, THE ISSUE RECURRED SEVERAL MINUTES AFTER RESTARTING THE UNIT. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: No Patient Involvement
MAUDE report 6311848 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K071318. One submission often covers many models, so check the product and lot details in each record.
- Z-1119-2020 · Jan 28, 2019 · TerminatedLivaNova Sorin Connect DPIII KOMPL. S5 REF 96-415-130, 2017-08-15, IPX1, RXOnly, (01)04033817901594 Product Usage: The S5 System is used to perform, control and monitor extracorp
- Z-2866-2016 · Aug 25, 2016 · TerminatedStckert S5 System, S5 Heart-lung machine, Cardiopulmonary bypass heart-lung machine console Product Usage: The Stckert S5 System is intended to be used during cardiopulmonary bypa
- Z-0856-2014 · Dec 4, 2013 · TerminatedS5/C5 Heart-lung machine Product Usage: The StOckert S5/ Sorin C5 System is intended to be used during cardiopulmonary bypass for procedures lasting six (6) hours or less.
- Z-0142-2014 · Sep 24, 2013 · TerminatedS5 Heart-lung machine, Stockert S5 System. Catalogue No: 48-30/40/50-00. The Stockert S5 System is intended to be used during cardiopulmonary bypass for procedures lasting six(6)
- Z-0274-2013 · Sep 19, 2012 · TerminatedS5 Mast Roller Pump 150, Item Number: 10-88-00 The Stockert S5/Sorin C5 System is intended to be used during cardiopulmonary bypass for procedures lasting six hours or less.
- Z-0275-2013 · Sep 19, 2012 · TerminatedSorin C5 Perfusion System, Item number 58-00-00 The Stockert S5/Sorin C5 System is intended to be used during cardiopulmonary bypass for procedures lasting six hours or less.
- Z-0272-2013 · Sep 19, 2012 · TerminatedS5 Double Roller Pump 85, Item Number: 10-85-00 The Stockert S5/Sorin C5 System is intended to be used during cardiopulmonary bypass for procedures lasting six hours or less.
- Z-0271-2013 · Sep 19, 2012 · TerminatedS5 Single Roller Pump 150, Item Number: 10-80-00 The Stockert S5/Sorin C5 System is intended to be used during cardiopulmonary bypass for procedures lasting six hours or less.
- Z-0273-2013 · Sep 19, 2012 · TerminatedS5 Mast Roller Pump 85, Item Number: 10-88-60 The Stockert S5/Sorin C5 System is intended to be used during cardiopulmonary bypass for procedures lasting six hours or less.
- Z-1328-2012 · Feb 23, 2012 · TerminatedControl panel for mast roller pump 85 The S5 Perfusion System is used to perform, control and monitor extracorporeal blood circulation during an operation for up to six (6) hours.
- Z-1325-2012 · Feb 23, 2012 · TerminatedS5 Single Roller Pump 150 The S5 Perfusion System is used to perform, control and monitor extracorporeal blood circulation during an operation for up to six (6) hours.
- Z-1327-2012 · Feb 23, 2012 · TerminatedControl panel for mast roller pump 150/85 The S5 Perfusion System is used to perform, control and monitor extracorporeal blood circulation during an operation for up to six (6) ho
- Z-1326-2012 · Feb 23, 2012 · TerminatedS5 Double Roller Pump 85 The S5 Perfusion System is used to perform, control and monitor extracorporeal blood circulation during an operation for up to six (6) hours.
Other CONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS devices
- Terumo® Advanced Perfusion System 1 801188Terumo Cardiovascular Systems Corporation · Console, Heart-Lung Machine, Cardiopulmonary Bypass3 recalls447 reports
- MAQUET CARDIOHELP CARDIOHELP-iMaquet Cardiopulmonary AG · CONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS5 recalls2 deaths64 reports
- MAQUET CARDIOHELP CARDIOHELP SystemMaquet Cardiopulmonary AG · CONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS4 recalls18 deaths107 reports
- Terumo® Advanced Perfusion System 1 816300Terumo Cardiovascular Systems Corporation · Console, Heart-Lung Machine, Cardiopulmonary Bypass300 reports
- Terumo® Advanced Perfusion System 1 816571Terumo Cardiovascular Systems Corporation · Console, Heart-Lung Machine, Cardiopulmonary Bypass230 reports
- Terumo® Advanced Perfusion System 1 801763Terumo Cardiovascular Systems Corporation · Console, Heart-Lung Machine, Cardiopulmonary Bypass1 death230 reports
- ESSENZ HLMLivaNova Deutschland GmbH · CONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS1 recall1 death110 reports
- Terumo® Advanced Perfusion System 1 5773Terumo Cardiovascular Systems Corporation · Console, Heart-Lung Machine, Cardiopulmonary Bypass1 recall78 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.