International safety notice
Lot Recall for the Profemur® AM Stem Ti Plasma, Wright Medical Technology Inc.
Germany / BfArM · DEU · Dec 29, 2011
Key facts
| Title | Lot Recall for the Profemur® AM Stem Ti Plasma, Wright Medical Technology Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Profemur® AM Stem Ti Plasma, Wright Medical Technology Inc. |
| Manufacturer | Lot Recall for the Profemur® AM Stem Ti Plasma, Wright Medical Technology Inc. |
| Models | 09112011, 20545, PRAMLH07, 01-901-867-4324, PRAMLH06, 0701150036, 0701148878 |
| Date | Dec 29, 2011 |
| 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