International safety notice
Batch Recall for the product E.Motion FP Meniscal component F5R 12mm, Aesculap AG
Germany / BfArM · DEU · Jul 14, 2014
Key facts
| Title | Batch Recall for the product E.Motion FP Meniscal component F5R 12mm, Aesculap AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the product E.Motion FP Meniscal component F5R 12mm, Aesculap AG |
| Manufacturer | Batch Recall for the product E.Motion FP Meniscal component F5R 12mm, Aesculap AG |
| Models | DE812160059, D-78532, 7461-95, 726261, DEUTDESS653, N0655, 78532, 78501, 00048719, 49174, 52000828, 65109852 |
| Date | Jul 14, 2014 |
| 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