International safety notice
Recall of several Zenith Ankle Tibial Inserts, Corin
Germany / BfArM · DEU · Dec 10, 2013
Key facts
| Title | Recall of several Zenith Ankle Tibial Inserts, Corin |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of several Zenith Ankle Tibial Inserts, Corin |
| Manufacturer | Recall of several Zenith Ankle Tibial Inserts, Corin |
| Models | 506.1122, 06.1051, 06.1063, 506.1073, 1910453, 506.1084, 506.1071, 06.1081, 506.1064, 506.1053, 506.1054, 506.1062 and 18 more |
| Date | Dec 10, 2013 |
| 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