International safety notice
Vástagos femorales modulares de cadera no cementados: Modulus, Modulus-R, Revision y vástagos femorales modulares de cadera cementados: Revision LR. Ver códigos afectados en el anexo 1 de la nota de aviso de la empresa.
Spain / AEMPS · ESP · Nov 21, 2019
Key facts
| Title | Vástagos femorales modulares de cadera no cementados: Modulus , Modulus-R , Revision y vástagos femorales modulares de cadera cementados: Revision LR. Ver códigos afectados en el anexo 1 de la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Vástagos femorales modulares de cadera no cementados: Modulus , Modulus-R , Revision y vástagos femorales modulares de cadera cementados: Revision LR. Ver códigos afectados en el anexo 1 de la nota de aviso de la empresa. |
| Manufacturer | Lima Corporate SPA, Italia. |
| Models | 3819.15.020, 7515.15.005, 4310.15.100, 4330.15.170, 7515.15.030, 7595.15.050, 3813.15.010, 3815.15.020, 4330.15.180, 3842.15.130, 3810.15.010, 7515.15.110 and 94 more |
| Event type | Safety Notice |
| Date | Nov 21, 2019 |
At a glance
- No Recall
- Yes Field safety notice
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