International safety notice
RemelTM E. coli Polyvalent Agglutinating sera
Czech / Ksrzis · CZE · Nov 15, 2019
Key facts
| Regulator | Czech / Ksrzis |
|---|---|
| Country | CZE |
| Brand | RemelTM E. coli Polyvalent Agglutinating sera |
| Manufacturer | Remel Europe Ltd, Velká Británie |
| Models | 2832563, 2514882, 2527762, 2510252, 01256, 2479722, 479525, R30954901, 694238, 2458666, 295600, 225413 |
| Event type | Safety Notice |
| Date | Nov 15, 2019 |
| 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