International safety notice
Equipos de contrapulsación Cardiosave Hybrid y Cardiosave Rescue. (Ver productos afectados en la nota de aviso de la empresa.)
Spain / AEMPS · ESP · Aug 22, 2023
Key facts
| Title | Equipos de contrapulsación Cardiosave Hybrid y Cardiosave Rescue. (Ver productos afectados en la nota de aviso de la empresa.) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Equipos de contrapulsación Cardiosave Hybrid y Cardiosave Rescue. (Ver productos afectados en la nota de aviso de la empresa.) |
| Manufacturer | Datascope Corp. Getinge, EEUU. |
| Models | 10607567113432, 10607567111117, 0998-00-0800-85, 2.1.9, 10607567111940, 0998-00-0800-53, 10607567108391, 07470, 91.822.52.89, 2023-394, 0998-00-0800-55, 96896 and 34 more |
| Event type | Safety Notice |
| Date | Aug 22, 2023 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 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