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The deadline to submit a claim in the Medtronic Sprint Fidelis Leads class action lawsuit is Monday. If you’re eligible to claim compensation in this class action lawsuit settlement you must submit a claim and supporting documentation by Sept. 28, 2020!

A $26 million settlement has been reached in a class action lawsuit alleging that Medtronic Sprint Fidelis Leads were prone to fracturing, potentially shocking patients and requiring replacement.

According to the class action, launched in 2009, patients implanted with pacemakers with Sprint Fidelis leads with model number 6949, 6948, 6931 or 6930 could experience unintended shocks due to fracturing of the leads.

Medtronic Sprint Fidelis Leads are devices used in implanted cardioverter/defibrillators, commonly known as pacemakers. The class action lawsuit alleged that certain leads manufactured by Medtronic and Medtronic Canada were defective.

A History of Problems with Medtronic Sprint Fidelis Leads

Medtronic and Medtronic Canada manufactured Sprint Fidelis Leads for use in defibrillators; however, the products faced a recall in 2007 after reports that the leads were prone to fracture surfaced.

According to the recall reports, some patients suffered severe injuries. Medtronic Sprint Fidelis Leads were not only included in pacemakers manufactured by Medtronic, as well as by other manufacturers.

As of 2010, nearly 270,000 Medtronic Sprint Fidelis Leads were reportedly implanted. According to a report in the Netherlands Heart Journal, even after Medtronic’s voluntary recall of the leads, additional complications were documented. These problems included lead failures, including decreases in signal amplitude, frequent short sensed intervals, and increased lead impedance.

Though the recall noted that the leads could be dangerous, patients were generally not advised to undergo surgery to remove the leads. Instead, patients with the leads were monitored closely and potentially have the lead capped. In some patients, removal of the pacemaker and replacement was the better option.

The Class Action Lawsuit and Settlement

In 2009, a class action lawsuit was certified in federal court in Canada. According to the complaint, the plaintiffs, along with other patients implanted with pacemakers containing the Medtronic Sprint Fidelis Leads were susceptible to unanticipated shocks and even have their device removed. Other injuries allegedly included strokes, pneumothorax, hemothorax, infections, and other complications. In addition, Class Members allegedly suffered minor injuries, including nerve injuries, pain, hematomas, and cellulitis.

The plaintiffs claimed that Medtronics misrepresented the safety of its Sprint Fidelis Leads to patients and healthcare providers.

In early 2020, the parties in the Medtronic Sprint Fidelis Leads class action lawsuit agreed to a $26 million settlement to end the litigation. These funds will go to qualifying patients implanted with the leads, as well as Public Health Insurers, and to pay the costs of the litigation and administration of the settlement.

The Medtronic Sprint Fidelis Leads class action settlement was approved by the Ontario Superior Court of Justice on April 1, 2020.

Under the terms of the agreement, Class Members can claim up to $25,000 under an Extraordinary Injury Fund established by the settlement, depending on the injuries they suffered related to the Medtronic Sprint Fidelis leads. These injuries include unintended shocks as well as minor or major injuries related to the removal or replacement of the lead.

Major injuries include:

  • Stroke
  • Pneumothorax
  • Hemothorax
  • Infection
  • Others

Minor injuries include:

  • Peripheral nerve injury
  • Cellulitis
  • Implant pain
  • Hematoma

Major or minor injuries must have occurred within 45 days of the Class Member’s surgery to replace or remove the Medtronic Sprint Fidelis Leads.

Class Members in the Medtronic Sprint Fidelis Leads class action settlement include patients implanted with pacemakers withs Sprint Fidelis leads with model number 6949, 6948, 6931 or 6930 and certain family members. The model number can be found on the implant card or obtained from the Class Member’s healthcare provider.

Class Members have until Sept. 28, 2020 to file a claim in the Medtronic Sprint Fidelis Leads settlement.

Who’s Eligible

Patients implanted with pacemakers with Sprint Fidelis leads with model number 6949, 6948, 6931 or 6930 and certain family members. The model number can be found on the implant card or obtained from the Class Member’s healthcare provider.

Potential Award

Up to $25,000

Class Members can claim up to $25,000 under an Extraordinary Injury Fund established by the settlement, depending on the injuries they suffered related to the Medtronic Sprint Fidelis leads. These injuries include unintended shocks as well as minor or major injuries related to the removal or replacement of the lead.

Proof of Purchase

Claimants will be asked to include documentation such as medical records and/or a physician declaration about the fracture or impending fracture of the lead.

Claim Form

NOTE: If you do not qualify for this settlement do NOT file a claim.

Remember: you are submitting your claim under penalty of perjury. You are also harming other eligible Class Members by submitting a fraudulent claim. If you’re unsure if you qualify, please read the FAQ section of the Settlement Administrator’s website to ensure you meet all standards (Top Class Actions is not a Settlement Administrator). If you don’t qualify for this settlement, check out our database of other open class action settlements you may be eligible for.

Claim Form Deadline

9/28/2020

Case Name

The Medtronic Sprint Fidelis Leads Class Action Lawsuit is Sherry Marie Robinson, et al. v. Medtronic Inc. and Medtronic of Canada Ltd., in the Ontario Superior Court of Justice, Canada.

Final Hearing

3/2/2020

Claims Administrator

Medtronic Leads Class Action Claims Administrator
P.O. Box 4454, Toronto Station A
25 The Esplanade, Toronto, ON M5W 4B1

Class Counsel

Joel P. Rochon
ROCHON GENOVA LLP

Megan B. McPhee
KIM SPENCER MCPHEE.

Defense Counsel

Danielle Royal

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Please note: Top Class Actions is not a settlement administrator or law firm. Top Class Actions is a legal news source that reports on class action lawsuits, class action settlements, drug injury lawsuits and product liability lawsuits. Top Class Actions does not process claims and we cannot advise you on the status of any class action settlement claim. You must contact the settlement administrator or your attorney for any updates regarding your claim status, claim form or questions about when payments are expected to be mailed out.

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4 Comments

  • HM December 13, 2020

    I just had a lead replaced last week. I just learned of the faulty leads in late November as I had vibrations in my chest due while driving my car. Upon going to the doctor, we realized that one of the leads needed to come out so I had surgery December 3rd, 2020. The leads were initially put in back in November of 2008 but I have never received any correspondence about a recall.

    Is there anything I can do at this point as I have just been made aware of this recall and class action suit.

  • Agnes Craine November 3, 2020

    Add me please

  • Anita Watson September 15, 2020

    Please add me.

  • mike jewett May 4, 2020

    I was poisened with many heavy metals at a battery factory in Calgary….Is there or has there ever been a suit for this?…I have been very ill since 1998…..thank you

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