Sheridan Endotracheal Tube Recall Issued After Four Patient Deaths
Following four patient deaths, a class I medical device recall for Sheridan Endotracheal Tubes has been announced because they can disconnect unexpectedly.
June 27, 2019 By: Martha Garcia
Following four patient deaths, a class I medical device recall for Sheridan Endotracheal Tubes has been announced because they can disconnect unexpectedly.
Bard claims two cases selected for the third and fourth bellwether trials are no longer representative of the litigation due to the plaintiffs' worsening injuries and need for additional surgeries due to their failed hernia mesh products.
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A federal judge has announced he will soon begin remanding 3M earplug lawsuits back to their originating districts for trials over claims of veteran hearing loss.