International safety notice
Corrective action for OPTI CCA-TS, OPTI CCA-TS2, OPTI CCA and OPTI-R analyzer, OPTI Medical Systems
Germany / BfArM · DEU · May 4, 2015
Key facts
| Title | Corrective action for OPTI CCA-TS, OPTI CCA-TS2 , OPTI CCA and OPTI-R analyzer, OPTI Medical Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | OPTI CCA-TS, OPTI CCA-TS2 , OPTI CCA and OPTI-R analyzer, OPTI Medical Systems |
| Manufacturer | Corrective action for OPTI CCA-TS, OPTI CCA-TS2 , OPTI CCA and OPTI-R analyzer, OPTI Medical Systems |
| Models | 30076, CCA-TS2, 770-510-4444, 2015-008US, 2015-008, 2015-006, GD7045, GD7031, GD7046, GD7013, 1-800-490-6784 |
| Date | May 4, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 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