International safety notice
Recall of two batches of the Neumann Titan Arthrodesis Plate Proximal, Zimmer GmbH on behalf of Normed Medizin-Technik GmbH
Germany / BfArM · DEU · Apr 20, 2015
Key facts
| Title | Recall of two batches of the Neumann Titan Arthrodesis Plate Proximal, Zimmer GmbH on behalf of Normed Medizin-Technik GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of two batches of the Neumann Titan Arthrodesis Plate Proximal, Zimmer GmbH on behalf of Normed Medizin-Technik GmbH |
| Manufacturer | Recall of two batches of the Neumann Titan Arthrodesis Plate Proximal, Zimmer GmbH on behalf of Normed Medizin-Technik GmbH |
| Models | 501007525, 2.12-1, 501007520, 2015-03 |
| Date | Apr 20, 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