International safety notice
Corrective action for the Amax Destiny Plus coagulation analyzers from Trinity Biotech
Germany / BfArM · DEU · Dec 19, 2006
Key facts
| Title | Corrective action for the Amax Destiny Plus coagulation analyzers from Trinity Biotech |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Amax Destiny Plus coagulation analyzers from Trinity Biotech |
| Manufacturer | Corrective action for the Amax Destiny Plus coagulation analyzers from Trinity Biotech |
| Models | 10.10, 111865, 2006SN002, 2769800, REFEAT9D, NO.2006SN002_P, NO.2C06SN002, 000219, 22906, 20.2.1, 239226, NO.2006SN002 and 1 more |
| Date | Dec 19, 2006 |
| 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