International safety notice
Alert 2818 (Technosurveillance) - VR Medical - Defibrillator/Monitor - Possibility of locking after application of defibrillation shock.
Brazil / Anvisa · BRA · Mar 18, 2019
Key facts
| Title | Alert 2818 (Technosurveillance) - VR Medical - Defibrillator/Monitor - Possibility of locking after application of defibrillation shock. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: Defibrillator/Monitor Technical Name: Automatic / Semi-Automatic External Defibrillator ANVISA registration number: 80102511541 Risk Class: III Affected model: LIFEPAK 15 Affected serial numbers: 42202343; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA CNPJ 04718143000194 RUA BATATAES 391 CONJUNTOS 11 12 E 13 SÃO PAULO SP TEL 11989257160 EMAIL CRISTIANEAGUIRREVRMEDICALCOMBR FABRICANTE DO PRODUTO PHYSIOCONTROL INC STRYKER 11811 WILLOWS ROAD NORTHEAST REDMOND WASHINGTON 98052 ESTADOS UNIDOS DA AMÉRICA |
| Models | 43928103, 43927351, 80102511541, 43926895, 43927223, 43928089, 43927701, 43927452, 42202343, 43927076, 43927669, 43927579 and 3 more |
| Date | Mar 18, 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