International safety notice
KODAK DirectView DR 7500 System
Spain / AEMPS · ESP · Jan 15, 2019
Key facts
| Title | KODAK DirectView DR 7500 System |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | KODAK DirectView DR 7500 System |
| Manufacturer | Carestream Health, Inc., EEUU. |
| Models | 28224, MA-2018-012, 0100-0944, 91.822.52.89, 2019-016, 48775, 28022, 2019PUEDE |
| Event type | Safety Notice |
| Date | Jan 15, 2019 |
At a glance
- No Recall
- Yes 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