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Genetown
FDA: Class I Recall for Medtronic, Inc.'s Physio-Control Defibs
July 7, 2010
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1 min read
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Mass Device -- Medtronic Inc. subsidiary Physio-Control's "field correction" for its LifePak 20/20e defibrillators is now a Class I recall, according to the Food & Drug Administration.
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Food and Drug Administration (FDA)
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