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: Colorado Springs Personal Injury LawyerMedtronic Defibrillator Leads Recalled
By Shannon Weidemann
Defibrillator leads that connect an implanted defibrillator have been recalled. The defective medical device is made by Medtronic and may cause the device to function incorrectly. The name of the product is Medtronic Sprint Fidelis Defibrillator Leads.
Full post as published by Colorado Springs Personal Injury Lawyer on October 22, 2007 (boomark / email).
Medtronic
Leads Failing
Medtronic Inc.
stents coated with contaminated heparin recalled
Medtronic CD Horizon
allegedly recalled as defective device for being prone to failure, shearing and cable breaks.
Advil - Ibuprofen
allegedly leads to Stevens Johnson Syndrome and Toxic Epidermal Necrosis.
Medtronic Kappa and Sigma Pacemakers
FDA Issues Class I Recall
Medtronic's Infuse Bone Graft
allegedly linked to life-threatening complications.
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