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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

Nov 2023: 0 reportsDec 2023: 2 reportsJan 2024: 1 reportsFeb 2024: 0 reportsMar 2024: 2 reportsApr 2024: 2 reportsMay 2024: 3 reportsJun 2024: 0 reportsJul 2024: 1 reportsAug 2024: 2 reportsSep 2024: 1 reportsOct 2024: 2 reportsNov 2024: 2 reportsDec 2024: 2 reportsJan 2025: 0 reportsFeb 2025: 2 reportsMar 2025: 0 reportsApr 2025: 1 reportsMay 2025: 1 reportsJun 2025: 1 reportsJul 2025: 1 reportsAug 2025: 1 reportsSep 2025: 2 reportsOct 2025: 1 reportsNov 2025: 0 reportsDec 2025: 1 reportsJan 2026: 1 reportsFeb 2026: 2 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520263
Last 36 months. The most recent month may be incomplete.

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.

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.

Other LivaNova Deutschland GmbH products

All LivaNova Deutschland GmbH devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page