International safety notice
Lot specific recall of the NexGen CRA/LCCK/RHK 5 mm Distal Femoral Augment, Size F, Zimmer
Germany / BfArM · DEU · Apr 23, 2015
Key facts
| Title | Lot specific recall of the NexGen CRA/LCCK/RHK 5 mm Distal Femoral Augment, Size F, Zimmer |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot specific recall of the NexGen CRA/LCCK/RHK 5 mm Distal Femoral Augment, Size F, Zimmer |
| Manufacturer | Lot specific recall of the NexGen CRA/LCCK/RHK 5 mm Distal Femoral Augment, Size F, Zimmer |
| Models | 2.12-1, 62815809, 00-5990-036-10, 1822565-03-24-2015-004-R, 2015-30 |
| Date | Apr 23, 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