International safety notice
Desfibriladores/Monitores Philips HeartStart XL+. Referencia: 861290, fabricados antes del 1 de mayo de 2017
Spain / AEMPS · ESP · Nov 13, 2019
Key facts
| Title | Desfibriladores/Monitores Philips HeartStart XL+. Referencia: 861290, fabricados antes del 1 de mayo de 2017 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Desfibriladores/Monitores Philips HeartStart XL+. Referencia: 861290, fabricados antes del 1 de mayo de 2017 |
| Manufacturer | Philips Medical Systems, EEUU |
| Models | 861290, FCO86100210, 91.822.52.89, “FCO86100210, 28050, 55753, 2019PUEDE, 28022, 5.416, FSN86100208A, 2019-594, A-28017143 |
| Event type | Safety Notice |
| Date | Nov 13, 2019 |
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