International safety notice
Prótesis Vario‐Cup-autocentrado,Cabeza protésica B,Sistema de prótesis de cadera LCU sin cementar,Componente tibial PS Gemini SL y Componente tibial de rotación Gemini SL
Spain / AEMPS · ESP · Nov 28, 2019
Key facts
| Title | Prótesis Vario‐Cup-autocentrado,Cabeza protésica B,Sistema de prótesis de cadera LCU sin cementar,Componente tibial PS Gemini SL y Componente tibial de rotación Gemini SL |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Prótesis Vario‐Cup-autocentrado,Cabeza protésica B,Sistema de prótesis de cadera LCU sin cementar,Componente tibial PS Gemini SL y Componente tibial de rotación Gemini SL |
| Manufacturer | Waldemar Link GmbH & Co. KG, Alemania |
| Models | 1938212, 318‐444, 2019-625, 107‐220, 1937251, 165‐013, 1937214, 1939263, 190218, 165‐016, 165-016, 128‐822 and 12 more |
| Event type | Safety Notice |
| Date | Nov 28, 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