Medtronic Lead Recall

Medtronic Lead Recall Center

Scientists are constantly working in respect to make the Medtronic lead recall treatment much more suffer, so that more number of people can make use of this treatment and get benefited through it.

In the light of recent events which lead to Medtronic recall action for their Sprint Fidelis products, Medtronic has already set up a recall center. It aims to help people who have suffered the ill-effects of defective Medtronic defibrillator leads as well as represent several of the families who have lost one of their family members when they were already in the process of filing class action lawsuit against Medtronic.

Helping them with the matters is Fields Law Firm, which is well-known as one of the most experienced and hard-working law-firms in Minnesota. This particular law firm has decided to fully devote its expertise for representing the injured individuals. Specialty attorneys like Medtronic lead recall attorney at this law firm are specifically trained for protecting individual interests and they can aptly handle Medtronic lawsuits providing personal attention and professionalism.

Almost all of the Medtronic Sprint Fidelis class action cases are being dealt in federal court of Minneapolis, Minnesota. As Medtronic itself is situated in Minnesota, this location is most suitable for dealing in the quickest possible way.

The Medtronic recall happened in 15th October 2007 due to the defective Sprint Fidelis leads and as much as five deaths were soon reported which were linked with these Medtronic leads. Estimated to be implanted in around 268000 patients worldwide the patients now face extraordinary situations.

Food and Drug Administration (FDA) and Medtronic have already advised all the patients to immediately consult with their physicians, in case they have the defective Sprint Fidelis leads. This is especially important if a patient undergoes fainting, lightheadedness and multiple shocks.

While it may appear to be tempting to undergo another implantation surgery to remove the faulty Sprint Fidelis leads, many physicians have already advised their patients NOT to undergo this surgery. A large number of complications may arrive whose risk factor is several times high than the defective Medtronic leads. Obviously, the patient remains in flux to decide whether to make do with the current fault leads or to take new risk of implanting a new lead.

One can always check if he/she has a defective Medtronic lead by simply tallying the lead number against the following numbers:

Sprint Fidelis 6949
Sprint Fidelis 6948
Sprint Fidelis 6931
Sprint Fidelis 6930

The Medtronic lawsuits are handled through a procedure known as multidistrict litigation (MDL, for short). Each case will be processed individually. All of the MDL cases are processed only till the discovery matters and then they are returned to the original court. The original court further processes the case once the discovery stage is done at MDL.

However risky the Medtronic leads are in their present condition, it should be noted that the risk of fracture is present almost in equal percent for other products as well. Alternative way to deal with the problems, such as re-programming of the defibrillator unit so as it keeps check on the false reading is better way. One can also cap the Medtronic lead and implant the new one.

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