International safety notice
Oclusor septal GORE CARDIOFORM, nº de catálogo GSXE0020, GSXE0025 y GSXE0030
Spain / AEMPS · ESP · Sep 21, 2021
Key facts
| Title | Oclusor septal GORE CARDIOFORM, nº de catálogo GSXE0020, GSXE0025 y GSXE0030 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Oclusor septal GORE CARDIOFORM, nº de catálogo GSXE0020, GSXE0025 y GSXE0030 |
| Manufacturer | W.L. GORE and Associates, Inc. Medical Products Division, EE.UU. |
| Models | 23569078, GSXE0025B, 00733132631025, 00733132617647, GSXE0030B, GSX0030A, 00733132631018, 32470, GSXE0020, 2021-525, 71943, 00733132617630 and 24 more |
| Event type | Safety Notice |
| Date | Sep 21, 2021 |
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