International safety notice
Recall of the products „ConMed Linvatec, Sterile, Ultra Power Burs, ConMed Linvatec E9000 Burs“ from ConMed Linvate
Germany / BfArM · DEU · Mar 30, 2007
Key facts
| Title | Recall of the products „ConMed Linvatec, Sterile, Ultra Power Burs, ConMed Linvatec E9000 Burs“ from ConMed Linvate |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the products „ConMed Linvatec, Sterile, Ultra Power Burs, ConMed Linvatec E9000 Burs“ from ConMed Linvate |
| Manufacturer | Recall of the products „ConMed Linvatec, Sterile, Ultra Power Burs, ConMed Linvatec E9000 Burs“ from ConMed Linvate |
| Models | BBC61779, BBC62649, 007021815, BBC73518, BBC62260, BBC62803, BBC60951, BBC64627, ВВС65927, BBC71992, BBC73560, BBC64626 and 911 more |
| Date | Mar 30, 2007 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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