International safety notice
Corrective action for the Kodak DirectView DR 9000 System, Carestream Health, Inc.
Germany / BfArM · DEU · Jul 1, 2014
Key facts
| Title | Corrective action for the Kodak DirectView DR 9000 System, Carestream Health, Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Kodak DirectView DR 9000 System, Carestream Health, Inc. |
| Manufacturer | Corrective action for the Kodak DirectView DR 9000 System, Carestream Health, Inc. |
| Models | 14608, MA-2014-005 |
| Date | Jul 1, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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