International safety notice
Recall for In-situ Bender/Cutter wide and narrow, Synthes
Germany / BfArM · DEU · May 25, 2009
Key facts
| Title | Recall for In-situ Bender/Cutter wide and narrow, Synthes |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | In-situ Bender/Cutter wide and narrow, Synthes |
| Manufacturer | Recall for In-situ Bender/Cutter wide and narrow, Synthes |
| Models | 530521S, 530.522S, R2009015, 530.521S |
| Date | May 25, 2009 |
| 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