Actos Recall -

: The FDA requires a "black box" warning—its strongest level—on the product label to alert patients to the risk of congestive heart failure . Major Legal Settlements

: Following a 2011 French study linking the drug to bladder cancer, medical authorities in France and Germany suspended or banned the use of Actos. ACTOS RECALL

While there have been significant legal and international developments, it is important to clarify that . : The FDA requires a "black box" warning—its