FREMONT, Calif., April 18, 2025 /PRNewswire/ -- 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 System (also known under the product name...
Hence then, the article about fda classifies q apel medical inc s worldwide medical device recall and discontinuation of its 072 aspiration system hippo as class i was published today ( ) and is available on PR Newswire ( Middle East ) The editorial team at PressBee has edited and verified it, and it may have been modified, fully republished, or quoted. You can read and follow the updates of this news or article from its original source.
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