International safety notice
Lot recall of specific knee, hip and nail implants, Zimmer Biomet
Germany / BfArM · DEU · Mar 23, 2017
Key facts
| Title | Lot recall of specific knee, hip and nail implants, Zimmer Biomet |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot recall of specific knee, hip and nail implants, Zimmer Biomet |
| Manufacturer | Lot recall of specific knee, hip and nail implants, Zimmer Biomet |
| Models | 2.12-1, CP04102, 00784301508, 00585205416, 00225250015, 00585205219, 16MMDX48CM, 16MMDX46CM, 00225248015, 00585205218, 00225748014, 15MMDX44CM and 43 more |
| Date | Mar 23, 2017 |
| 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