International safety notice
Alert 2760 (Technosurveillance) - Stryker do Brasil - Visum Led Suspension - Visum Surgical Lights - Possibility that the EDS Suspension Light, Central Axis, has an insufficiently assembled connection.
Brazil / Anvisa · BRA · Jan 9, 2019
Key facts
| Title | Alert 2760 (Technosurveillance) - Stryker do Brasil - Visum Led Suspension - Visum Surgical Lights - Possibility that the EDS Suspension Light, Central Axis, has an insufficiently assembled connection. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Visum Surgical Lights - Visum Led Suspension Technical Name: Surgical Focus ANVISA registration number: 80005430286 Risk Class: I Affected model: Visum Led Suspension Affected serial numbers: 14E007088; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO STRYKER DO BRASIL CNPJ 02966317000102 RUA URUSSUÍ 300 7º ANDAR SÃO PAULO SP TEL 11 51892550 EMAIL QUALIDADESTRYKERCOM FABRICANTE DO PRODUTO STRYKER COMMUNICATION 1410 LAKESIDE PARKWAY FLOWER MOUND ESTADOS UNIDOS |
| Models | 80005430286, 14E007098, 14F001748, 14E007088 |
| Date | Jan 9, 2019 |
| 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