International safety notice
Destornillador DVR® Crosslock ePAKTM, referencia 212000002; Medidor de profundidad DVR® Crosslock ePAKTM, referencia 212000003;Aguja Kirschner con Punta Trocar, referencia 212000008
Spain / AEMPS · ESP · Jul 5, 2019
Key facts
| Title | Destornillador DVR® Crosslock ePAKTM, referencia 212000002; Medidor de profundidad DVR® Crosslock ePAKTM, referencia 212000003;Aguja Kirschner con Punta Trocar, referencia 212000008 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Destornillador DVR® Crosslock ePAKTM, referencia 212000002; Medidor de profundidad DVR® Crosslock ePAKTM, referencia 212000003;Aguja Kirschner con Punta Trocar, referencia 212000008 |
| Manufacturer | Biomet Inc., EEUU. |
| Models | 2019-361, 08038, 28022, 2029.LA, CF04108, 212000002, CP04102, 53138, 212000008, 2024.AGUJA, 2.12-1, 91.822.52.89 and 4 more |
| Event type | Safety Notice |
| Date | Jul 5, 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