Guidant Exec Reportedly Knew Of Problems
According to a law firm web site quoting the Associated Press, Guidant executive Fred McCoy admitted that the company had not received FDA approval before fixing a problem with the company's Ventak Prizm 2 Model 1861.
Consumer Help Web has reported on the organization's continuing problems throughout the latest round of recalls and warnings. If you have a Guidant device installed, please talk with your physician.
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