International safety notice
Recall for the Juggerknot System, BIOMET
Germany / BfArM · DEU · Aug 15, 2011
Key facts
| Title | Recall for the Juggerknot System, BIOMET |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Juggerknot System, BIOMET |
| Manufacturer | Recall for the Juggerknot System, BIOMET |
| Models | 800-348-9500, 574-371-3756, FDA-0178, 912000, 20852-9787, 574-371-3755, FDA-1088 |
| Date | Aug 15, 2011 |
| 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