International safety notice
Alert 2956 (Technosurveillance) - Air Liquide - Monnal T75 Ventilator, Monnal T75 CO2 Lung Ventilator Possibility of failure to increase PEEP when Pressure Support is not greater than 2 cmH2O in PSV, PSV NIV and PS PRO ventilation modes.
Brazil / Anvisa · BRA · Aug 21, 2019
Key facts
| Title | Alert 2956 (Technosurveillance) - Air Liquide - Monnal T75 Ventilator, Monnal T75 CO2 Lung Ventilator Possibility of failure to increase PEEP when Pressure Support is not greater than 2 cmH2O in PSV, PSV NIV and PS PRO ventilation modes. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Monnal T75 CO2 Lung Ventilator (registration 80204410032); Technical Name: Pressure and Volume Ventilator ANVISA registration number: 80204410032; Risk Class: III Affected model: Monnal T75 CO2 KB033600 and Monnal T75 KB022600 Affected serial numbers: See attachment List of serial numbers at risk. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO AIR LIQUIDE DO BRASIL LTDA CNPJ 00331788000119 AVENIDA MORUMBI 8234 3º ANDAR SÃO PAULO SP TEL 61 3568 5666 EMAIL CAMILARODRIGUESAIRLIQUIDECOM FABRICANTE DO PRODUTO AIR LIQUIDE MEDICAL SYSTEMS 6 RUE GEORGES BESSE FRANÇA TEL 33 0140966600 ALMEDICALSYSTEMSVIGILANCEAIRLIQUIDECOM |
| Models | 80204410015, KB022600, 80204410032, KB033600 |
| Date | Aug 21, 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