International safety notice
Productos implantables e instrumentos para traumatología Biomet, fabricados antes de marzo de 2018, que figuran en el anexo 2-Lista de productos de la Nota de Aviso de la empresa.
Spain / AEMPS · ESP · Oct 25, 2019
Key facts
| Title | Productos implantables e instrumentos para traumatología Biomet, fabricados antes de marzo de 2018, que figuran en el anexo 2-Lista de productos de la Nota de Aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Productos implantables e instrumentos para traumatología Biomet, fabricados antes de marzo de 2018, que figuran en el anexo 2-Lista de productos de la Nota de Aviso de la empresa. |
| Manufacturer | Biomet Orthopedics, EEUU. |
| Models | 760180, 745970, 300260, PM156684, 276900, 677870, 706510, PM0001086, 300230, PM555404, 847240, 21-123212 and 3100 more |
| Event type | Safety Notice |
| Date | Oct 25, 2019 |
At a glance
- No Recall
- Yes Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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