International safety notice
• Sistema transfemoral de balón expandible SOLOPATH. • Sistema de balón replegable SOLOPATH. Ver modelos afectados en la nota de aviso de la empresa.
Spain / AEMPS · ESP · May 21, 2019
Key facts
| Title | • Sistema transfemoral de balón expandible SOLOPATH. • Sistema de balón replegable SOLOPATH. Ver modelos afectados en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | • Sistema transfemoral de balón expandible SOLOPATH. • Sistema de balón replegable SOLOPATH. Ver modelos afectados en la nota de aviso de la empresa. |
| Manufacturer | Terumo Medical Corporation, USA. |
| Models | 2019-05, STFI-1625, STFI-1435, SR-2435, STFI-2135, 91.822.52.89, STFI-1925, SR-2235, SR-2025, SR-2035, STFI-2125, STFI-1425 and 13 more |
| Event type | Safety Notice |
| Date | May 21, 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