International safety notice
Alert 2503 (Technosurveillance) - Fresenius - Equipo Volumat Agilia VL ON70 Occurrence of alerts ERROR 24 during pump adjustment
Brazil / Anvisa · BRA · Feb 28, 2018
Key facts
| Title | Alert 2503 (Technosurveillance) - Fresenius - Equipo Volumat Agilia VL ON70 Occurrence of alerts ERROR 24 during pump adjustment |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Equipo Volumat Agilia VL ON70 Technical name: Equipment ANVISA registration number: 80145110199 Risk class: III Affected model: VL ON 70 Affected serial number: 32342397 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO FRESENIUS KABI BRASIL LTDA CNPJ 49324221000104 AV MARGINAL PROJETADA 1652 BARUERI SÃO PAULO FABRICANTE CLINICO MEDICAL SPZ O O BLONIE K BLONIE KWROCLAWIA UL ROBERTA KOCHA I MIEKINIA 55330 POLONIA TELEFONE 11 25041481 FAX 11 25041602 TELEFONE CINTIAGARCIAFRESENIUSKABICOM |
| Models | 80145110199, 32342397 |
| Date | Feb 28, 2018 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 1–9 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