- #MEDTRONIC PASSMAKER BATTERY RECALL PROFESSIONAL#
- #MEDTRONIC PASSMAKER BATTERY RECALL SERIES#
- #MEDTRONIC PASSMAKER BATTERY RECALL FREE#
Notably, significant injury or death if cardiac arrest occurs and cannot be treated in time. This follows Abbott Laboratories recalling their pacemakers (Assurity and Endurity) just the month before in March 2021.Īnd, before that, on 2 nd December, Boston Scientific recalled their implantable heart defibrillator, the EMBLEM.įailure of any of these devices has highly significant consequences. In addition, the protection of our clients’ personal information is governed by GMP privacy policy (the “Privacy Policy”), as follows:GMP Privacy Policy assures you as an existing or future client, that in retaining our services to represent you or your business, the entire GMP team will handle your file in accordance with this policy pursuant to all applicable Federal and Provincial legislation including, but not limited to, the Personal Information Protection and Electronic Documents Act (”PIPEDA”).In April 2021, Medtronic PLC, a medical device manufacturer, issued an urgent safety alert for both their implantable pacemaker devices (Evera, Viva, Brava, Claria, Amplia, Compia and Visia) and their implantable defibrillators.
#MEDTRONIC PASSMAKER BATTERY RECALL PROFESSIONAL#
It is upon this fundamental principle that our firm adheres to the Law Society of Upper Canada’s Rules of Professional Conduct regarding the security of our clients’ personal information, common law principles of solicitor-client privilege and, where applicable, litigation-privilege. GREG MONFORTON & PARTNERS and MONFORTON, ROBITAILLE & BEZAIRE, PROFESSIONAL CORPORATION (both entities hereinafter referred to as “GMP”) recognize and respect their clients’ personal information and endeavour to safeguard that information from unauthorized use, retention, or disclosure to third parties.
#MEDTRONIC PASSMAKER BATTERY RECALL FREE#
We are representing clients throughout Canada.įor free answers to your questions about the Medtronic class action lawsuit, call us at (866) 320-4770. If you or a loved one has been injured by a defective Medtronic heart defibrillator or pacemaker, we encourage you to contact us. on behalf of Canadians injured by potentially defective heart defibrillators and pacemakers. Greg Monforton and Partners is handling legal claims against Medtronic, Inc. If you have received a Medtronic defibrillator or pacemaker and are unsure whether your device is covered by the warning, you should call your physician to determine whether or not the information regarding this notification applies to you. Medtronic recommends patients with potentially defective devices discuss possible explanation with their physicians. This advisory covers approximately 28,000 pacemakers. Medtronic warned that a wire problem in the pacemaker could cause symptoms such as dizziness or fainting in some patients.
#MEDTRONIC PASSMAKER BATTERY RECALL SERIES#
The warning from Medtronic also included the Sigma series pacemakers. The warning affects approximately 87,000 Medtronic defibrillators, and more than 13,000 people with these ICDs already have had the devices surgically removed. This lawsuit covers all Canadians who received a defective Medtronic defibrillator manufactured between April 2001 and December 2003. Medtronic Class Action LawsuitĪ class action lawsuit is pending in Canada seeking $170,000,000 in damages for Canadians injured by defective Medtronic defibrillators. The subject devices were manufactured between April 2001 and December 2003. This design defect can lead to rapid battery depletion.Īs a result of the defect, many people are being advised to have their Medtronic devices surgically removed. The defibrillator and pacemaker devices subject to this warning are vulnerable to an internal short. warned patients that certain defibrillator and pacemaker devices manufactured by the company have a potentially serious defect that can render the devices inoperable.
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