International safety notice
Corrective Action for Cholestech LDX, Alere
Germany / BfArM · DEU · Jul 11, 2012
Key facts
| Title | Corrective Action for Cholestech LDX, Alere |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Cholestech LDX, Alere |
| Manufacturer | Corrective Action for Cholestech LDX, Alere |
| Models | V3.40, 877-308-8289, 44444, 49-51162628630 |
| Date | Jul 11, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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