Overview of recall records associated with Maquet Cardiopulmonary Ag, including dates, categories and classifications where available.
Classification mix: Class II: 5.
HKH 8820 Wall Holder does not comply with standard DIN EN 1789:20 and has the potential to detach.
This lot of arterial cannula may have been supplied with 3/8-width de-airing plugs that could break during the process of removal from the arterial cannula.
This lot of arterial cannula may have been supplied with 3/8-width de-airing plugs that could break during the process of removal from the arterial cannula.
This lot of arterial cannula may have been supplied with 3/8-width de-airing plugs that could break during the process of removal from the arterial cannula.
There is a possibility for the clamps of the gas bottle holder to crack or break when exposed to strong vibrations.
This page summarizes recall records in which the official source identifies Maquet Cardiopulmonary Ag 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.
