International safety notice
Diagnostické zdravotnické prostředky in vitro
Czech / Ksrzis · CZE · Jan 14, 2019
Key facts
| Title | Diagnostické zdravotnické prostředky in vitro |
|---|---|
| Regulator | Czech / Ksrzis |
| Country | CZE |
| Brand | Dimension Vista®, Affected Product: Millipore Progard Pretreatment Pack (Inteligentní laboratorní systémy Dimension Vista®) |
| Manufacturer | Siemens Healthcare Diagnostics Inc., USA |
| Models | F8BA35774, F7MA50339, F8JA97876, F8DA59251, VI19-01.A.OUS, F7MA56608, F8BA20457, F8AA13966, F8AA93567, F8HA79819, 10450564, F8MA06374 and 5 more |
| Event type | Safety Notice |
| Date | Jan 14, 2019 |
| Regulator page | eregpublicsecure.ksrzis.cz |
At a glance
- No Recall
- Yes 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