International safety notice
Alert 2513 (Technovigilance) - MDT - Products in sterile condition manufactured between 03/01/2013 and 10/01/2017 Change in the shade of the product stability indicator
Brazil / Anvisa · BRA · Mar 12, 2018
Key facts
| Title | Alert 2513 (Technovigilance) - MDT - Products in sterile condition manufactured between 03/01/2013 and 10/01/2017 Change in the shade of the product stability indicator |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Sterile products manufactured between 03/01/2013 and 10/01/2017 Technical name: N/A ANVISA registration number: N/A Risk class: III Affected model: N/A Affected serial number: All batches supplied in sterile condition (gamma radiation) manufactured in the period from 03/01/2013 to 10/01/2017. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO MDT INDUSTRIA COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO DE IMPLANTES SA AVENIDA BRASIL 2983 DISTRITO INDUSTRIAL SÃO CLARO SP FABRICANTE MDT INDUSTRIA COMÉRCIO IMPORTAÇÃO E EXPORTAÇÃO DE IMPLANTES SA AVENIDA BRASIL 2983 DISTRITO INDUSTRIAL BRASIL TELEFONE 19 21116500 FAX 19 21116500 EMAIL JMAXIMOVINCULACOMBR |
| Date | Mar 12, 2018 |
| 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