News

Pharmabiz3h
US FDA classifies Q’Apel Medical Inc.’s worldwide medical device recall and discontinuation of its 072 Aspiration System (Hippo) as Class I
Fremont, California Monday, April 21, 2025, 18:00 Hrs [IST] ...
MassDevice4h
FDA says Q’Apel aspiration system recall is Class I following discontinuation
Q’Apel Medical announced that the FDA classified a voluntary recall of its 072 A System as Class I, the most serious kind.