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FDA Alerts

FDA Discourages Use of Ultrasonic Aspirators for Uterine Fibroid Removal

In a guidance statement released October 30, the U.S. Food and Drug Administration (FDA) made a non-binding recommendation that the...

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First DePuy Attune Lawsuit Filed Alleging The Attune Knee Replacement Failed Prematurely

Please Note: CSS Firm is no longer accepting or investigating new DePuy Attune knee implant claims at this time. This...

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Lawmakers Consider Proposal to Delay Reporting of Medical Device Malfunctions

Despite the fact that medical device malfunctions often lead to severe patient injury or even death, the U.S. Food and...

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DePuy Attune Knee Systems May be Prone to Failure

Please Note: CSS Firm is no longer accepting or investigating new DePuy Attune knee implant claims at this time. This...

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Limited Voluntary Recall of Stryker LFIT Anatomic Cobalt Chromium V40 Femoral Head

The Stryker LFIT Anatomic Cobalt Chromium (CoCr) V40 femoral head had a limited voluntary recall in August, 2016, which can...

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Mylan’s Woes Continue: EpiPen and EpiPen Jr. Recall Announced

The U.S. Food and Drug Administration (FDA), is alerting consumers that Meridian Medical Technology is voluntarily recalling 13 lots of...

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GAO Says FDA Misjudged Risk Associated with Power Morcellator

The Government Accountability Office has issued a report stating that the U.S. Food and Drug Administration (FDA) underestimated the harmful...

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FDA Issues Draft Guidelines Regarding Off-Label Use of Drugs and Devices

According to a 2007 JAMA report, up to 75 percent of the cancer drugs used in the U.S. are prescribed...

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FDA to Speed Up Device Recall Notices

In the interest of increased consumer awareness, the U.S. Food and Drug Administration (FDA) recently announced that the agency will...

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FDA Recommends Boxed Warning, Patient Checklist for Essure

The U.S. Food and Drug Administration (FDA) has recommended a boxed warning for Bayer’s Essure, along with the inclusion of...

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