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Pharmabiz3 天
US FDA classifies Q’Apel Medical Inc.’s worldwide medical device recall and ...
Fremont, California Monday, April 21, 2025, 18:00 Hrs [IST] ...
MassDevice3 天
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.
FDA Classifies Q'Apel Medical Inc.'s Worldwide Medical Device Recall and Discontinuation of ...
On April 7, 2025, the U.S. Food and Drug Administration ("FDA" or "the agency"), classified Q'Apel Medical, Inc.'s ("Q'Apel" or "the company") voluntary recall of 1,617 units of its 072 Aspiration ...