International safety notice
Technical name: Non-modular stem for hip arthroplasty
Brazil / Anvisa · BRA · Oct 6, 2017
Key facts
| Title | Technical name: Non-modular stem for hip arthroplasty |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Beaded Femoral Stem FC 6" 14/15/16/17/18x160mm Technical name: Non-modular stem for hip arthroplasty ANVISA registration number: 80245480039 Risk class: III Affected model: 7843-14-06, 7843-15-06, 7843-16-06, 7843-17-06, 7843-18-06, 7843-20-06. Affected serial numbers: 784301706 107163; 784301806 62034164; 784301506 62143767; 784301606 62147264; 784301606 62147264; 784301406 62271353; 784301406 62302689; 784301506 62335828; 784301506 62379188; 784301506 62445614; 784301506 62445614; 784301506 53493900; 784301606 57912000; 784301406 60329445; 784301706 60946005; 784301806 60966723; 784301606 61000224; 784301506 61040238; 784301506 61198821; 784301406 61215303; 784301406 61215303; 784301506 63730100 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO WM WORLD MEDICAL IMP EXP LTDA CNPJ 03179994000143 RUA DO REZENDE 189 RIO DE JANEIRO RJ FABRICANTE ZIMMER INC WARSAW 1 ESTADOS UNIDOS |
| Models | 62147264, 784301706, 7843-18-06, 7843-15-06, 61198821, 61250415, 61215303, 61040238, 61714435, 7843-17-06, 61886033, 784301406 and 34 more |
| Date | Oct 6, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 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