International safety notice
Alert 2530 (Technosurveillance) - Wright - Valor®-Ankle Fusion Rod System Absence of compression screw, which may result in inappropriate joint compression.
Brazil / Anvisa · BRA · Mar 28, 2018
Key facts
| Title | Alert 2530 (Technosurveillance) - Wright - Valor®-Ankle Fusion Rod System Absence of compression screw, which may result in inappropriate joint compression. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Valor®-Ankle Fusion Rod System Technical name: Orthopedic Fixation Systems and Associated Devices ANVISA registration number: 80491360036 Risk class: III Affected model: 415101020R; Affected serial numbers: 1608296; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO WRIGHT MEDICAL BRASIL LTDA ME CNPJ 08051626000139 RUA JOAQUIM FLORIANO N 466 ANDAR 15 E 21 CONJ 1505 2111 E 2112 ITAIM BIBI CEP 04534002 SÃO PAULO SP FABRICANTE WRIGHT MEDICAL TECHNOLOGY INC 1023 CHERRY ROAD MEMPHIS TN 38117 ESTADOS UNIDOS MATTHEWPARRISHWRIGHTCOM |
| Models | 1608296, 80491360036, 415101115R, 1610957, 415101020R |
| Date | Mar 28, 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