International safety notice
Componentes de prótesis articulares. Gamas de producto Scorpio, Duracon, PCA y Trident. Ver nºs de referencia afectados en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Jan 11, 2024
Key facts
| Title | Componentes de prótesis articulares. Gamas de producto Scorpio, Duracon, PCA y Trident. Ver nºs de referencia afectados en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Componentes de prótesis articulares. Gamas de producto Scorpio, Duracon, PCA y Trident. Ver nºs de referencia afectados en la nota de aviso de la empresa. |
| Manufacturer | Stryker Joint Replacement, EEUU. |
| Models | 07613327034790, 6742-1-416, 54184201, 07613327033854, 3044-0028, 36273601, 04546540306388, 04546540305831, 3052-0515, PVDYTEN1, 04546540307101, 54537601 and 201 more |
| Event type | Safety Notice |
| Date | Jan 11, 2024 |
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