Datascope Corp.
15 Law Dr, FAIRFIELD, NJ, US
Registered product codes
4 product codes
Recent MDR events
48,537 on file
- CS300 Intra-Aortic Balloon Pump, English, 220VJul 31, 2026Malfunction2249723-2026-0003665
- System, Balloon, Intra-Aortic And ControlJul 31, 2026Malfunction2249723-2026-0003666
- CS300 Intra-Aortic Balloon Pump, English, 220VJul 31, 2026Malfunction2249723-2026-0003667
- CARDIOSAVE HYBRID, TYPE G PLUGJul 31, 2026Malfunction2249723-2026-0003668
- CARDIOSAVE HYBRID, TYPE B PLUGJul 31, 2026Malfunction2249723-2026-0003669
- Linear 7.5Fr. 34cc IAB with Accessories, US OnlyJul 31, 2026Malfunction2248146-2026-0001349
- CARDIOSAVE HYBRID, TYPE I PLUGJul 31, 2026Malfunction2249723-2026-0003670
- CARDIOSAVE HYBRID, TYPE B PLUGJul 31, 2026Malfunction2249723-2026-0003671
- Balloon CatheterJul 31, 2026Malfunction2248146-2026-0001350
- CARDIOSAVE HYBRID, TYPE G PLUGJul 31, 2026Malfunction2249723-2026-0003672
Recalls
94 on file
- Open, ClassifiedMar 19, 2026
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.
View FDA record ↗ - Open, ClassifiedMar 3, 2026
The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.
View FDA record ↗ - Open, ClassifiedMar 3, 2026
The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.
View FDA record ↗ - Open, ClassifiedDec 16, 2025
The IFU addendum updates the Vibration and Shock Table to reference the correct standards.
View FDA record ↗ - Open, ClassifiedDec 16, 2025
The IFU addendum updates the Vibration and Shock Table to reference the correct standards.
View FDA record ↗ - Open, ClassifiedDec 11, 2025
The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
View FDA record ↗ - Open, ClassifiedDec 11, 2025
The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
View FDA record ↗ - Open, ClassifiedNov 5, 2024
There is discrepant labeling on the inner and outer packaging of the device.
View FDA record ↗ - Open, ClassifiedSep 20, 2024
Firm has developed a software correction (Revision D.00) outside the US to mitigate product problems that pose a risk of hemodynamic instability and failure of transmission of clinical data in Cardiosave Hybrid and Cardiosave Rescue Intra-Aortic Balloon Pump devices.
View FDA record ↗ - Open, ClassifiedSep 20, 2024
Firm has developed a software correction (Revision D.00) outside the US to mitigate product problems that pose a risk of hemodynamic instability and failure of transmission of clinical data in Cardiosave Hybrid and Cardiosave Rescue Intra-Aortic Balloon Pump devices.
View FDA record ↗
Compliance history
Matched by FEI 1000222374.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.