International safety notice
Infusion bomb
Brazil / Anvisa · BRA · Jun 9, 2015
Key facts
| Title | Infusion bomb |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | PLUM XL family infusion pump, Registration nº 80253310022; |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL HOSPIRA PRODUTOS HOSPITALARES LTDA CNPJ 06283144000189 ENDEREÇO AV ENG LUIS CARLOS BERRINI Nº 901 CIDADE MONÇÕES SÃO PAULO SÃO PAULO TELEFONE 11 55083102FABRICANTE HOSPIRA INC EUA |
| Models | 80253310022 |
| Date | Jun 9, 2015 |
| 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