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Home » St. Jude Recalls Heart Occluder Tool, 483 Prompts FOIA Suit Against FDA
St. Jude Recalls Heart Occluder Tool, 483 Prompts FOIA Suit Against FDA
February 15, 2013
St. Jude Medical is recalling a tool used to implant Amplatzer heart hole closure devices due to a potentially flawed wire, a notice posted Tuesday to the FDA’s website says.