International safety notice
Alert 2809 (Technosurveillance) - Baxter Hospitalar - Colleague Volumetric Infusion Pump Need to carry out dielectric testing on specific devices.
Brazil / Anvisa · BRA · Mar 11, 2019
Key facts
| Title | Alert 2809 (Technosurveillance) - Baxter Hospitalar - Colleague Volumetric Infusion Pump Need to carry out dielectric testing on specific devices. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: Colleague Volumetric Infusion Pump Technical Name: Infusion Pump ANVISA registration number: 10068390320 Risk Class: III Affected model: Colleague 3 CXE Volumetric Infusion Pump/ Colleague CXE Volumetric Infusion Pump Affected serial numbers: 22070570DC; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BAXTER HOSPITALAR CNPJ 49351786000180 AVENIDA DR CHUCRI ZAIDAN Nº 1240 TORRE B 12º ANDAR VILA SÃO FRANCISCO SÃO PAULO SP TEL 11 56948877 EMAIL CINTIAGUEDESBAXTERCOM FABRICANTE DO PRODUTO BAXTER HEALTHCARE SA SINGAPORE BRANCH 2 WOODLANDS INDUSTRIAL PARK D STREET 2 CINGAPURA |
| Models | 22070570DC, 22060247UC, 10068390320 |
| Date | Mar 11, 2019 |
| 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