International safety notice
Recall of the Persona EM Proximal Tube and Persona EM Distal Rod, Zimmer Biomet
Germany / BfArM · DEU · Dec 14, 2015
Key facts
| Title | Recall of the Persona EM Proximal Tube and Persona EM Distal Rod, Zimmer Biomet |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the Persona EM Proximal Tube and Persona EM Distal Rod, Zimmer Biomet |
| Manufacturer | Recall of the Persona EM Proximal Tube and Persona EM Distal Rod, Zimmer Biomet |
| Models | 2.12-1, 62137112, 62156914, 62222598, 42-5399-001-00, 62137111, 2015-149, 62156913, 42-5399-002-00, 62222599 |
| Date | Dec 14, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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