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 JET 7
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 Xtra
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
Medication errors can create countless devastating impacts that can be long-term, serious, debilitating, and may even cause death. There are more than 100,000 medication errors reported
Asbestos is a grouping of 6 natural minerals that are made of soft, flexible fibers. These fibers are resistant to corrosion, heat, fire, and electricity. Although
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