International safety notice
Recall of CLINITEST hCG kit, Siemens Healthcare
Germany / BfArM · DEU · Jan 25, 2012
Key facts
| Title | Recall of CLINITEST hCG kit, Siemens Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of CLINITEST hCG kit, Siemens Healthcare |
| Manufacturer | Recall of CLINITEST hCG kit, Siemens Healthcare |
| Models | 031924, 031662, 877-229-3711, 030998, 029997, 030826, 2011-03-25, GPF-003-6, 032106, 031798, 27151, 030602 and 12 more |
| Date | Jan 25, 2012 |
| 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