International safety notice
FIBRINOGEN/FIBRIN DEGRADATION PRODUCT (FDP)
Brazil / Anvisa · BRA · Mar 13, 2013
Key facts
| Title | FIBRINOGEN/FIBRIN DEGRADATION PRODUCT (FDP) |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | VIDAS D-DIMER EXCLUSION II - Registration 10158120656 - Affected lot: 1001399220. UPDATE - 05/14/2013 - This Field Action was expanded to lots 1001408170/1001479890/1001531500/1001632240/1001743 890/1001820290 and 1001860670. |
| Manufacturer | DETENTOR DO REGISTRO DO PRODUTO NO BRASIL BIOMERIEUX BRASIL SA RIO DE JANEIRORJ |
| Models | 10158120656, 1001408170, 1001531500, 1001632240, 1001399220, 1001743890, 1001479890, 1001820290, 1001860670 |
| Date | Mar 13, 2013 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No 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