International safety notice
Recall of several models and lot mumbers of the Arthro-Knife, ConMed Linvatec
Germany / BfArM · DEU · Aug 31, 2009
Key facts
| Title | Recall of several models and lot mumbers of the Arthro-Knife, ConMed Linvatec |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of several models and lot mumbers of the Arthro-Knife, ConMed Linvatec |
| Manufacturer | Recall of several models and lot mumbers of the Arthro-Knife, ConMed Linvatec |
| Models | E6888, 99E88088, 09806888, ZZ0088, Z6EZ888, 900088, 996Z088, 99E6Z088, 09099088, E8088, 99EN088, 08088 and 403 more |
| Date | Aug 31, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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