Overview of recall records associated with Maquet Cardiopulmonary Gmbh, including dates, categories and classifications where available.
Classification mix: Class II: 5.
The packaging may not consistently maintain sterile barrier integrity.
The packaging may not consistently maintain sterile barrier integrity.
The packaging may not consistently maintain sterile barrier integrity.
Internal investigations have identified an issue with the durability of the connecting cable near the connection to the Venous Bubble Sensor. Excessive bending of the connecting cable can…
Device does not comply with the labeling requirements of international standard IEC 60601-1.
This page summarizes recall records in which the official source identifies Maquet Cardiopulmonary Gmbh 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.
