On December 15, 2020, the U.S. Food and Drug Administration (FDA) notified the public that Penumbra, Inc. had issued a voluntary recall of their Penumbra
The Food and Drug Administration (FDA) announced today that Penumbra has recalled all units of the Penumbra Reperfusion Catheter with Xtra Flex Technology (Jet 7
Hip replacements are among the most common orthopedic procedures in the United States. The operation is performed more than 300,000 times in the United States
Johnson & Johnson announced today it was discontinuing sales of its talc-based baby powder products in the United States and Canada amid a firestorm of
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