Maquet Cardiovascular AXIUS Blower Mister Product Code/REF Number: CB-1000 The Axius Blower recall — FDA Z-0983-2019
Potential lack of carbon dioxide (CO2) flow that may result in a procedural delay during off-pump coronary artery bypass (OPCAB).
Overview of recall records associated with Maquet Cardiovascular, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 237, Class I: 4.
Potential lack of carbon dioxide (CO2) flow that may result in a procedural delay during off-pump coronary artery bypass (OPCAB).
This page summarizes recall records in which the official source identifies Maquet Cardiovascular, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.