International safety notice
CARDIOSAVE Hybrid Intra-Aortic Balloon Pump
Swiss / SwissMedic · CHE · Feb 21, 2024
Key facts
| Title | CARDIOSAVE Hybrid Intra-Aortic Balloon Pump |
|---|---|
| Regulator | Swiss / SwissMedic |
| Country | CHE |
| Brand | CARDIOSAVE Hybrid Intra-Aortic Balloon Pump |
| Manufacturer | Datascope Corp. |
| Models | 10607567109053N, 10607567109008S.O, 10607567109053S.O, 10607567108391N, 0998-00-0800-530998-UC-0800-53, 10607567108414N, 10607567111117, 10607567109053, 10607567112312, 0998-UC-0800-52, 28.02.2023, 0998-00-0800-32 and 36 more |
| Event type | Safety Notice |
| Date | Feb 21, 2024 |
| Regulator page | fsca.swissmedic.ch |
At a glance
- No Recall
- Yes Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1