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.
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.
