International safety notice
Recall for Troponin I Rapid Test Devices and Myoglobin/CK-MB/Troponin I Combo Test Devices, DIMA
Germany / BfArM · DEU · Oct 21, 2008
Key facts
| Title | Recall for Troponin I Rapid Test Devices and Myoglobin/CK-MB/Troponin I Combo Test Devices, DIMA |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Troponin I Rapid Test Devices and Myoglobin/CK-MB/Troponin I Combo Test Devices, DIMA |
| Manufacturer | Recall for Troponin I Rapid Test Devices and Myoglobin/CK-MB/Troponin I Combo Test Devices, DIMA |
| Models | ROBERT-BOSCH4BREITE, 37079, 01551 |
| Date | Oct 21, 2008 |
| 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