International safety notice
Cardiosave Hybrid/Rescue Intra-Aortic Balloon Pump FSN 1, Cardiosave Hybrid/Rescue Intra-Aortic Balloon Pump Addendum
Ireland / HPRA · IRL · Nov 1, 2018
Key facts
| Title | Cardiosave Hybrid/Rescue Intra-Aortic Balloon Pump FSN 1, Cardiosave Hybrid/Rescue Intra-Aortic Balloon Pump Addendum |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | Cardiosave Hybrid/Rescue Intra-Aortic Balloon Pump FSN 1 Cardiosave Hybrid/Rescue Intra-Aortic Balloon Pump Addendum |
| Manufacturer | Maquet |
| Models | 0070-00-0638-21, 381–975, 7.11.1項, 0070-00-0637-14, 0070-00-0638-15, 0070-00-0638-17, 0070-00-0637-09, 795–676, 0070-00-0638-09, 250–5, CS300, 0070-00-0637-01 and 65 more |
| Event type | Safety Notice |
| Date | Nov 1, 2018 |
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