International safety notice
DEVICES
Brazil / Anvisa · BRA · Mar 5, 2012
Key facts
| Title | DEVICES |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | MULTIPACK FOR OPTISTAR MR - Registration 80136710130 - VAZ 60ml Syringe - AFFECTED LOTS: 0130214; MULTIPACK FOR OPTISTAR LE - Registration 80136710127 - VAZ 60ml Syringe - AFFECTED LOTS: 0008414; |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL MALLINCKRODT DO BRASIL LTDA AV DAS NAÇÕES UNIDAS 23130 SÃO PAULOSP FONEFAX 11218762731121876225 |
| Models | 1063220, 1049313, 0235011, 0078240, 1056021, 1098211, 80136710130, 1035287, 9114151, 0300142, 9275102, 0246197 and 36 more |
| Date | Mar 5, 2012 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers 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