International safety notice
Corrective action for Pentra 120, Pentra 120 retic, Pentra DX 120 and Pentra DF 120, Axon Lab
Germany / BfArM · DEU · Apr 20, 2006
Key facts
| Title | Corrective action for Pentra 120, Pentra 120 retic, Pentra DX 120 and Pentra DF 120, Axon Lab |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Pentra 120, Pentra 120 retic, Pentra DX 120 and Pentra DF 120, Axon Lab |
| Manufacturer | Corrective action for Pentra 120, Pentra 120 retic, Pentra DX 120 and Pentra DF 120, Axon Lab |
| Models | 9226-26, 9226-0, 322614977, D-73262 |
| Date | Apr 20, 2006 |
| 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