International safety notice
Sistemas del dispositivo Precice Intra-medullary limb lengthening (IMLL): • Precice IMLL • Precice Short Ver listado de productos afectados en el documento adjunto a la nota de aviso de la empresa.
Spain / AEMPS · ESP · Dec 22, 2021
Key facts
| Title | Sistemas del dispositivo Precice Intra-medullary limb lengthening (IMLL): • Precice IMLL • Precice Short Ver listado de productos afectados en el documento adjunto a la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas del dispositivo Precice Intra-medullary limb lengthening (IMLL): • Precice IMLL • Precice Short Ver listado de productos afectados en el documento adjunto a la nota de aviso de la empresa. |
| Manufacturer | NuVasive, Inc., EEUU |
| Models | PA0901-50Q150, PA1225-425, TSA4.5-020, PA1221-035, LSB5-055, PP1742-030, PA1223-000, PA0411-80A335, PA0465-80B335, PP1794-060, PA0411-50E230, HEC2-000 and 789 more |
| Event type | Safety Notice |
| Date | Dec 22, 2021 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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