International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Jan 23, 2020
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | IMMULITE 2000/IMMULITE 2000 XPi EBV-VCA IgM |
| Manufacturer | Siemens Healthcare Diagnostics Inc., USA |
| Models | 2020-01-31, 20-03, 10488005LOT, IMC20-03.A.OUS, 10488005, 2019-08-21, IMC2003.A.OUS, L2KEM2 |
| Event type | Safety Notice |
| Date | Jan 23, 2020 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes 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