International safety notice
Alert 2523 (Technosurveillance) - Baxter - Colleague Volumetric Infusion Pump Anticipation of preventive maintenance of the device
Brazil / Anvisa · BRA · Mar 16, 2018
Key facts
| Title | Alert 2523 (Technosurveillance) - Baxter - Colleague Volumetric Infusion Pump Anticipation of preventive maintenance of the device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Colleague Volumetric Infusion Pump Nome técnico: Colleague Single Channel Cxe Pump Portuguese V1.7, Colleague Triple Channel Cxe Pump Portuguese V1.7, Colleague Single Channel Mono Chrome Pump, Portuguese V1.7, Colleague Triple Channel Mono Chrome Pump Portuguese V1.7 ANVISA registration number: 10068390320 Risk class: III Affected model: BRM91617, BRM91637, BRM81517, BRM81537 Affected serial number: 23040120UP; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BAXTER HOSPITALAR CNPJ 49351786000180 AV DR CHUCRI ZAIDAN 1240 12º ANDAR TORRE B VILA SÃO FRANCISCO SÃO PAULO SP FABRICANTE BAXTERHEALTHCARE AS SINGAPORE BRANCH 2 WOODLANDS INDUSTRIAL PARK D STREET 2 SINGAPORE 737778 SINGAPURA |
| Models | 25040164UP, 25040017DP, 25040063DP, 25040181UP, 23050472UP, 25040027UP, 24030147UP, 25040162UP, 23050521UP, 25040022DP, 22070081UC, 25040165UP and 55 more |
| Date | Mar 16, 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