International safety notice
Desfibriladores externos automáticos (DEA) modelos Telefunken “HR1” y “FA1” y HeartReset, fabricados después del 18 de julio de 2016.
Spain / AEMPS · ESP · Aug 9, 2019
Key facts
| Title | Desfibriladores externos automáticos (DEA) modelos Telefunken “HR1” y “FA1” y HeartReset, fabricados después del 18 de julio de 2016. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Desfibriladores externos automáticos (DEA) modelos Telefunken “HR1” y “FA1” y HeartReset, fabricados después del 18 de julio de 2016. |
| Manufacturer | Defiteq International B.V., Holanda, ó GGT Holding B.V., Holanda |
| Models | “HR1”, 28022, 91.822.52.89, “FA1”, 33005, 2019-457, 2017.A |
| Event type | Safety Notice |
| Date | Aug 9, 2019 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 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