Some defectives guidewires manufactured by Medtronic can cause serious injury or death. The voluntary recall initiated by Medtronic in October was recently classified as a Class I recall by the US FDA.
Guidewires are inserted in arteries to guide and place stents. Those being recalled have a coating that can break off and block a blood vessel.
Medtronic initiated the recall after four problems were reported including one patient who suffered cardiac arrest but was resuscitated according to WebMD
New York Personal Injury Attorneys Blog


Central Line-Associated Bloodstream Infections (CLABSI) are often the result of medical malpractice. An estimated 250,000 CLABSIs occur every year in the US with 800,000 of them happening in the emergency room. More than 30,000 people die from CLABSI in the US every year. The CDC estimates that the yearly cost related to CLABSI is $1 billion.
Volkswagen is recalling several popular models for the the following reasons: