FDA Classifies Q'Apel Medical Worldwide Medical Device Recall and Discontinuation of Its 072 Aspiration System (Hippo) as Class I
April 19, 2025
April 19, 2025
WASHINGTON, April 19 -- The U.S. Department of Health & Human Services' Food and Drug Administration issued the following recall notice:
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FDA Classifies Q'Apel Medical Inc.'s Worldwide Medical Device Recall and Discontinuation of its 072 Aspiration System (Hippo) as Class I
Company Announcement
Fremont, CA - April 18, 2025 - On April 7, 2025, the U.S. Food and Drug Administration ("FDA" or "the agency" . . .
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FDA Classifies Q'Apel Medical Inc.'s Worldwide Medical Device Recall and Discontinuation of its 072 Aspiration System (Hippo) as Class I
Company Announcement
Fremont, CA - April 18, 2025 - On April 7, 2025, the U.S. Food and Drug Administration ("FDA" or "the agency" . . .