International safety notice
Corrective action for the Tytin Regular Set, Kerr Corporation
Germany / BfArM · DEU · Jun 30, 2014
Key facts
| Title | Corrective action for the Tytin Regular Set, Kerr Corporation |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Tytin Regular Set, Kerr Corporation |
| Manufacturer | Corrective action for the Tytin Regular Set, Kerr Corporation |
| Models | 3‐1294, 29948, 00800 |
| Date | Jun 30, 2014 |
| 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