International safety notice
Corrective action for the diagnostic ultrasound system ProSound F75, Hitachi Aloka Medical, Ltd.
Germany / BfArM · DEU · Jul 29, 2014
Key facts
| Title | Corrective action for the diagnostic ultrasound system ProSound F75, Hitachi Aloka Medical, Ltd. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the diagnostic ultrasound system ProSound F75, Hitachi Aloka Medical, Ltd. |
| Manufacturer | Corrective action for the diagnostic ultrasound system ProSound F75, Hitachi Aloka Medical, Ltd. |
| Models | 202M4893, 202M4901, 81-422-45-6049, 202M4883, 202M4898, 202M4882, 202M4891, 202M4900, 202M4874, 202M4877, 202M8849, 202M4896 and 12 more |
| Date | Jul 29, 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