International safety notice
Alert 2561 (Technosurveillance) GE Healthcare do Brasil - Ultrasound System Risk of electric shock.
Brazil / Anvisa · BRA · May 4, 2018
Key facts
| Title | Alert 2561 (Technosurveillance) GE Healthcare do Brasil - Ultrasound System Risk of electric shock. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Ultrasound System (ANVISA Registration 80035360066); Technical name: Ultrasound System ANVISA registration number: 80035360066; Risk class: II Affected model: Logiq 9 Affected batch/series numbers: equipment installed since April 2015 or that had its power cable replaced since April 2015. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOHOSPITALARES LTDA CNPJ 00029372000140 AV MAGALHÃES DE CASTRO Nº 4800 11º ANDAR CIDADE JARDIM SÃO PAULO SP TEL 11 30678436 EMAIL TECNOVIGILANCIABRGECOM FABRICANTE GE MEDICAL SYSTEMS ULTRASOUND PRIMARY CARE DIAGNOSTICS LLC 9900 INNOVATION DRIVE WAUWATOSA WISCONSIN 53226 EUA |
| Models | 80071260361, 80071260187, 80035360066, 80071260207, 80071260213 |
| Date | May 4, 2018 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 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