International safety notice
CARDIOSAVE Hybrid Intra-Aortic Balloon Pump
Swiss / SwissMedic · CHE · Jun 27, 2019
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 | 0998-00-0800-XX, 0998-00-3013-XX, D998-00-0800-XX, CS100, 07470, CPBIACS100, D998-UC-0800-XX, 0998-UC-0800-XX, IABPCS100, D998-00-3023-XX, 0998-00-3023-XX, RescueCS300 and 7 more |
| Event type | Safety Notice |
| Date | Jun 27, 2019 |
| Regulator page | fsca.swissmedic.ch |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching catalog numbers in FDA data
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