International safety notice
Technical name: Virus
Brazil / Anvisa · BRA · Oct 25, 2016
Key facts
| Title | Technical name: Virus |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Two products are affected by Campo’s action: 1. Commercial name: RUBELLA IGM IMMULITE / IMMULITE 1000 Technical name: Rubella Virus Registration 10345160740 Affected batch(es): 333 and 334. /// 2. Trade name: RUBEOLA IgM IMMULITE 2000 Registration 10345160813 - Affected lots: 237, 236M, 238, 239 /// Risk Class: III - Products that present a high risk to the user, the patient and/or public health |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULOSP 11 39083877 CAROLINEHAYASHIDASIEMENSCOM FABRICANTE SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD GLYN RHONWY LLANBERIS GWYNEDD LL55 4EL REINO UNIDO |
| Models | 10345160813, 10345160740 |
| Date | Oct 25, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No 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