International safety notice
Lot Recall of the Versys® Hip System Cemented Revision/Calcar Femoral Stem, Versys Heritage® Hip Prosthesis Femoral Revision Stem, Zimmer Inc.
Germany / BfArM · DEU · Dec 3, 2013
Key facts
| Title | Lot Recall of the Versys® Hip System Cemented Revision/Calcar Femoral Stem, Versys Heritage® Hip Prosthesis Femoral Revision Stem, Zimmer Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot Recall of the Versys® Hip System Cemented Revision/Calcar Femoral Stem, Versys Heritage® Hip Prosthesis Femoral Revision Stem, Zimmer Inc. |
| Manufacturer | Lot Recall of the Versys® Hip System Cemented Revision/Calcar Femoral Stem, Versys Heritage® Hip Prosthesis Femoral Revision Stem, Zimmer Inc. |
| Models | 61282897, 60829410, 60864621, 00370166, 61433840, 60745880, 61304639, 61886910, 60889541, 61977880, 60821283, 60768910 and 875 more |
| Date | Dec 3, 2013 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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