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This system analyzes publicly available FDA MAUDE data. It does NOT provide medical advice. MAUDE data is de-identified — do not attempt re-identification. © 2026 Claripulse.

Back to Mechanical Circulatory Support
MAUDE LookupMechanical Circulatory SupportCS300 Intra-Aortic Balloon Pump, Italian, 220V

CS300 Intra-Aortic Balloon Pump, Italian, 220V Adverse Events: FDA MAUDE Data

Datascope Corp. · Intra-Aortic Balloon Pump System (IABP) · First cleared Jun 1989

Total Reports

206

Reports (30d)

5

Active Signals

1

Open Recalls

85

Monthly Report Volume
Event Type Breakdown

What the reports describe · Claripulse analysis

Most commonly reported problems

1

Battery Not Charging During Use

battery, balloon pump, patient involved, cardiosave intra, pump iabp

5

reports

2

Touch Screen Not Working

balloon pump, screen, cardiosave, cardiosave intra, pump iabp

2

reports

3

Autofill Failure Alarm

balloon pump, autofill, autofill failure, failure alarm, pump iabp

1

reports

4

Helium Leak Issue

pump iabp, helium, balloon pump, leak, cardiosave intra

1

reports

5

Template Summary: N/A

1

reports

6

Unit Not Switching On During Check

battery, routine, patient involved, routine check, patient reported

1

reports

Problem groupings are generated by Claripulse from report narrative text. They summarize what reporters wrote, not adjudicated root cause.

Detection

Active safety signals

Disproportionate reportinghigh

Regulatory

FDA recalls for this device

Class III

Feb 6, 2026 · Open, Classified

The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to operate the IABP. Getinge has identified that a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging. The right bay of the Battery Charging Station is not affected by this issue.

Class II

Jan 23, 2026 · Open, Classified

The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.

Class II

Jan 23, 2026 · Open, Classified

The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.

Class II

Nov 4, 2025 · Open, Classified

The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.

Class II

Nov 4, 2025 · Open, Classified

The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.

Class III

Oct 23, 2025 · Open, Classified

The IFU addendum updates the Vibration and Shock Table to reference the correct standards.

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Understanding this data

What FDA MAUDE data does and does not tell you

How these reports are filed, why raw counts mislead, and the limits to know before drawing conclusions.

→

How a safety signal is detected

What the "Active Signals" count above means and the methods that separate a real signal from noise.

→
Disclaimer: This system analyzes publicly available FDA MAUDE data. It does NOT provide medical advice. MAUDE data is de-identified. Do not attempt re-identification. Report counts may differ from the FDA's MAUDE search due to processing cadence and deduplication. Data is updated weekly.