International safety notice
Recall of the ACT-LR-cuvettes, Technidyne Corporation
Germany / BfArM · DEU · Jun 29, 2005
Key facts
| Title | Recall of the ACT-LR-cuvettes, Technidyne Corporation |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the ACT-LR-cuvettes, Technidyne Corporation |
| Manufacturer | Recall of the ACT-LR-cuvettes, Technidyne Corporation |
| Models | 08820, 1-732-548-9824, 732.632.9299, 732.548.5700, 1-800-631-5945, 800.6316945 |
| Date | Jun 29, 2005 |
| 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