Recall: 15,355 results found.
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Sprint Fidelis Lead Recall | Beasley Allen
On October 15, 2007, Medtronic suspended sale of their Sprint Fidelis Defibrillator leads (Models 6930, 6931, 6948, 6949) after receiving reports of 5 fatalities. According to Medtronic, since 2004 over 268,000 patients in the United States have been implanted with the defective lead as part of the defibrillator.
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