International safety notice
Technical name: Non-modular stem for hip arthroplasty
Brazil / Anvisa · BRA · May 31, 2017
Key facts
| Title | Technical name: Non-modular stem for hip arthroplasty |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Zimmer Non-Cemented Hip Femoral Component Technical name: Non-modular stem for hip arthroplasty ANVISA registration number: 80175510040 Risk class: III Affected model: 00-7843-014-06, 00-7843-015-06, 00-7843-016-06, 00-7843-017-06, 00-7843-018-06 and 00-7843-020-06 Affected serial numbers: Lot - 62067453 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO PORTOMED COMERCIO E REPRESENTAÇÃO DE MATERIAIS ORTOPÉDICOS LTDA RUA COSTA Nº 238 MENINO DEUS CEP 90110270 PORTO ALEGRE RS FONEFAX 051 21179999 CNPJ 03992299000104 FABRICANTE ZIMMER INC 1800 WEST CENTER STREET WARSAW INDIANA 46580 |
| Models | 00-7843-016-06, 00-7843-015-06, 00-7843-020-06, 00-7843-014-06, 00-7843-017-06, 62067453, 00-7843-018-06, 80175510040 |
| Date | May 31, 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