International safety notice
Recall of all lots of T.E.S.S. Glenoid Anatomic Polyethylene Inlay, Biomet
Germany / BfArM · DEU · Mar 26, 2012
Key facts
| Title | Recall of all lots of T.E.S.S. Glenoid Anatomic Polyethylene Inlay, Biomet |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of all lots of T.E.S.S. Glenoid Anatomic Polyethylene Inlay, Biomet |
| Manufacturer | Recall of all lots of T.E.S.S. Glenoid Anatomic Polyethylene Inlay, Biomet |
| Models | 700340, 700341, 700343, 700342 |
| Date | Mar 26, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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