International safety notice
Alert 2844 (Technosurveillance) - Stryker do Brasil LTDA - Exeter System Models removed from registry 80005430008.
Brazil / Anvisa · BRA · Apr 15, 2019
Key facts
| Title | Alert 2844 (Technosurveillance) - Stryker do Brasil LTDA - Exeter System Models removed from registry 80005430008. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: Exeter System Technical Name: Total Hip Prostheses ANVISA registration number: 80005430008 Risk Class: III Model affected: Various models. Affected serial numbers: All sold from 2015-2019 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO STRYKER DO BRASIL LTDA CNPJ 02966317000102 RUA URUSSUÍ 300 8º ANDAR SÃO PAULO SP TEL 11 51892550 EMAIL QUALIDADESTRYKERCOM FABRICANTE DO PRODUTO HOWMEDICA OSTEONICS CORP 325 CORPORATE DRIVE MAHWAH NJ 07430 |
| Models | 2015-2019, 80005430008 |
| Date | Apr 15, 2019 |
| 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