International safety notice
CLINITEK Status, CLINITEK Status+, and CLINITEK Status Connect Systems
Ireland / HPRA · IRL · Oct 2, 2014
Key facts
| Title | CLINITEK Status, CLINITEK Status+, and CLINITEK Status Connect Systems |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | CLINITEK Status, CLINITEK Status+, and CLINITEK Status Connect Systems |
| Manufacturer | Siemens Healthcare Diagnostics |
| Models | 10379680, 10309178, 15140, 20140, 10379675, 10376324, 08140, GPF-003, 10379681, 13140, 10140, 21140 and 36 more |
| Event type | Recall |
| Date | Oct 2, 2014 |
| Regulator page | hpra.ie |
At a glance
- Yes Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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