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Medtronic Insulin Pumps Tied to Serious Injury

Recalled Medtronic Insulin Pumps – What They Knew, When They Knew It

Recalls seem to be all over the news from children’s toys that can cause choking hazards to car parts that can crack and lead to accidents. However, these important notices shouldn’t be ignored or put off, especially if it involves a medical device that you are using on a daily basis. Recently, several models of Medtronic insulin pumps were recalled and failure to correct this problem could lead to serious injuries or even death for diabetic patients.

What They Knew

MiniMed insulin pumps are about the size of a small cell phone and are usually worn on a belt or stored in a pocket. This device is necessary for certain diabetes patients because it delivers much needed insulin to keep the body working properly. Unfortunately, incident reports have been filed alerting that many patients are experiencing infusion set tubing blockages which can deliver too much or not enough insulin. The wrong insulin levels can cause fainting, seizures, a coma or even death. This has caused the FDA to issue a Class 1 recall which is the most urgent.

When They Knew It

On September 12, 2017, the FDA announced that Medtronic is conducting a voluntary recall of specific lots of infusion sets used with all models of Medtronic insulin pumps. However, this is hardly the first time Medtronic has been in the news for faulty insulin pumps.

In 2009, Medtronic was required to perform its first recall by the FDA of its Quick-set infusion sets because these models were known to deliver improper insulin doses. In 2013, Medtronic issued another recall, this time for The SynchroMed II and SynchroMed EL Implantable Drug Infusion Pumps. Additionally, the FDA wrote a warning letter to Medtronic stating that their quality control inspection did not pass and that there were many violations committed in their factory.

What Can You Do?

Medtronic is no stranger to the legal system. Over the last five years they have been taken to court many times on behalf of injured patients and families whose loved ones have died due to malfunctioning insulin pumps. If you or a loved one suffered from hypoglycemia, ketoacidosis, other diabetic related injuries or death because of a faulty Medtronic insulin pump, you may be able to make a legal claim against Medtronic. For years they have been distributing problematic devices that have caused life threatening injuries. Contact us today to see if you are entitled to financial compensation to help pay for your medical bills, lost wages and other fees you may have accumulated.

Medtronic Warnings In The News

9/11/17: Medtronic Announces Voluntary Recall of Diabetes Infusion Sets

Medtronic plc (NYSE:MDT) announced today that it has started to inform patients worldwide of a voluntary recall of specific lots of infusion sets used with all models of Medtronic insulin pumps. The recall is related to a certain discontinued component in these infusion sets and does not include insulin pumps or glucose sensors.

The company determined, through recent field reports from patients and root cause analysis, that a component, the vent membrane, in the recalled infusion sets may be susceptible to being blocked by fluid during the process of priming/fill-tubing. This situation can lead to potential over-delivery of insulin shortly after an infusion set change, which may cause hypoglycemia.

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8/10/17: Medtronic Recall of Diabetes Infusion Sets

Medtronic determined through recent field reports from patients and root cause analysis that the vent membrane in the recalled infusion sets may be susceptible to being blocked by fluid during the process of priming/fill-tubing. This situation can lead to potential over-delivery of insulin shortly after an infusion set change, which may cause hypoglycemia.

Medtronic recommends that customers use only infusion sets made with the new and enhanced component, the membrane, starting with their next set change. Medtronic would like to remind customers that it is very important to carefully follow the Key Steps document included with the recall notification letter regarding the priming/fill-tubing process – especially if a person only has recalled infusion sets.

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Filed Medtronic Complaints & Damages

2/15/17: Brackin V. Medtronic Minimed, Inc.

This action arises out of the death of Plaintiff Bryan Brackin’s wife, Pamela W. Brackin (hereinafter “Pam Brackin” for convenience) on January 22, 2016, after a MiniMed Paradigm REAL-Time Revel Insulin Pump, model/item number MMT-523RNAS, serial number PAR706522U and/or its related equipment infused an overdose of insulin into Pamela Brackin, causing her to become severely hypoglycemic and suffer hypoglycemic coma resulting in her death.

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GET YOUR Medtronic Insulin Pumps CASE REVIEW TODAY

Medtronic settlements are now being negotiated, but there is a limited window to pursue help. If you think you, a friend, or a family member may qualify, get your free case review today… before it’s too late!

  • * Submit now to learn if you may be eligible for a cash settlement or call (800) 511-3838 now.

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The Step-By-Step Guide To Taking Action

How to File for Financial Settlement After Injury from an Unsafe Drug or Device

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Periscope Group is not owned by or operated on behalf of any attorney or law firm. We are not affiliated with any drug or medical device companies. We do not host advertisements nor do we accept advertising requests. We are here to help YOU, the consumer, become better educated and supported. You pay absolutely nothing for our help. It’s as simple as that.

Periscope Group is not owned by or operated on behalf of any attorney or law firm. We are not affiliated with any drug or medical device companies. We do not host advertisements nor do we accept advertising requests. We are here to help YOU, the consumer, become better educated and supported. You pay absolutely nothing for our help. It’s as simple as that.

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© All Rights Reserved • 2017 • Periscope Group, 4155 Blackhawk Plaza Circle, Suite 100, Danville, CA 94506 Legal Disclaimer

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