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E/P Pack UPS ModuleRecalls & 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 04033817901259), received between Oct 19, 2016 and Mar 10, 2023 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Device Operational Issue” (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.

Most reported problems

Device problems

  • Device Operational Issue1
  • Electrical Power Problem1
  • Electrical Shorting1
  • Failure to Power Up1
  • Smoking1

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.

  • MalfunctionMar 10, 2023Smoking; Smoking

    SEE INITIAL REPORT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16520055 ↗
  • MalfunctionSep 20, 2017Device Operational Issue; Device Operational Issue

    LIVANOVA (B)(4) RECEIVED A REPORT THAT AN S5 UPS MODULE WAS FOUND TO BE FAULTY WHEN THE DEVICE WAS STARTED DURING SETUP. IF THE DEVICE WAS SWITCHED TO UPS MODE, THE DISPLAY MODULE WOULD TURN ON AND OFF. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Patient Involvement

    MAUDE report 6881062 ↗
  • MalfunctionOct 19, 2016Failure to Power Up; Electrical Power Problem; Electrical Shorting; Failure to Power Up; Electrical Power Problem; Electrical Shorting

    SORIN GROUP (B)(4) RECEIVED A REPORT THAT A BAD SMELL CAME FROM THE SORIN S5 SYSTEM WHEN IT WAS SWITCHED ON WITHOUT AC POWER DURING A DEMONSTRATION. THE S5 SYSTEM WAS SWITCHED OFF AND BACK ON USING AC POWER AND THE UNIT DISPLAYED MULTIPLE ERROR MESSAGES. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Patient Involvement

    MAUDE report 6040500 ↗

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 · Terminated
    LivaNova 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 · Terminated
    Stckert 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 · Terminated
    S5/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 · Terminated
    S5 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-0273-2013 · Sep 19, 2012 · Terminated
    S5 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-0275-2013 · Sep 19, 2012 · Terminated
    Sorin 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-0274-2013 · Sep 19, 2012 · Terminated
    S5 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-0272-2013 · Sep 19, 2012 · Terminated
    S5 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 · Terminated
    S5 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-1325-2012 · Feb 23, 2012 · Terminated
    S5 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-1326-2012 · Feb 23, 2012 · Terminated
    S5 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.
  • Z-1328-2012 · Feb 23, 2012 · Terminated
    Control 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-1327-2012 · Feb 23, 2012 · Terminated
    Control 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

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.