International safety notice
Technical name: Modular stem for hip arthroplasty
Brazil / Anvisa · BRA · Dec 27, 2017
Key facts
| Title | Technical name: Modular stem for hip arthroplasty |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Zimmer Cemented Hip Femoral Component Technical name: Modular stem for hip arthroplasty ANVISA registration number: 80175510036 Risk class: III Affected model: 00-8114-002-00 Affected serial numbers: Lot - 62268572, 62273048, 62275085, 62277490, 62333960, 62370965, 62370971, 62370975, 62370978 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO PORTOMED COMÉRCIO E REPRESENTAÇÕES DE MATERIAIS ORTOPÉDICOS LTDA CNPJ 03992299000104 RUA COSTA 238 PORTO ALEGRE RS FABRICANTE ZIMMER INC 1800 WEST CENTER STREET EUA TELEFONE 305 2696315 EMAIL FNCNEMEAAMERICAS FNCNEMEAAMERICASZIMMERBIOMETCOM |
| Models | 62370978, 80175510036, 62370971, 62370965, 62370975, 62275085, 62333960, 62273048, 62277490, 00-8114-002-00, 62268572 |
| Date | Dec 27, 2017 |
| 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