International safety notice
Treadmill
Brazil / Anvisa · BRA · Feb 24, 2015
Key facts
| Title | Treadmill |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Exercise Treadmill, Risk Class I, Model: T2100, Brand: GE Healthcare, Registration: 80071260189, T2100 Exercise Treadmills that use power cables with the following part numbers: 408930-001 REV E - manufactured from June 1, 2006 until December 10, 2014. If the cable is marked RWK, it means that it has already been inspected (SEE LETTER TO THE CUSTOMER) /// 408930-002 REV C manufactured from June 1, 2006 until January 19, 2015. /// 2028038-008 REV B - manufactured from December 1, 2006 until January 28, 2015. |
| Manufacturer | DETENTOR DO REGISTRO GE HEALTHCARE DO BRASIL COM E SERV PARA EQUIPAMENTOS MÉDICOHOSPITALARES LTDA CNPJ 00 029 372 0001 40 ENDEREÇO AV MAGALHÃES DE CASTRO Nº 4800 13º ANDAR CIDADE JARDIM SÃO PAULO SP FABRICANTE GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES INC ESTADOS UNIDOS 8200 TOWER AVENUE MILWAUKEEWI |
| Models | 2028038-008, T2100, 80071260189, 408930-001, 408930-002 |
| Date | Feb 24, 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