Medtronic Minimed Insulin Pump Lawsuit
Around 400,000 people use insulin pumps each day in the United States. The devices, which can be used in lieu of a daily injection, can help those with diabetes achieve a better quality of life and provide reassurance that they are getting the insulin they need in the right doses. Yet if these pumps are defective in any way, the consequences can be dangerous, even deadly. That seems to be the case with a large number of Medtronic MiniMed Insulin Pumps, which had to be taken off the market after the FDA issued a recall. Many of those affected by the defective insulin pumps have filed lawsuits against Medtronic, with numerous claims that the MiniMed insulin pumps have caused serious injury and fatalities. Medtronic insulin pump lawyers are now asking for others to come forward to begin their compensation claims if these faulty devices have injured them or a loved one.
If you have been harmed by using Medtronic MiniMed insulin pump, Select Justice can help fight for your rights and compensation.
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Medtronic Insulin Pumps Lawsuit
Have you or a Loved One Been Injured as a Result of Using a Medtronic Insulin Pump?
At John Bales Attorneys we have dedicated our lives to fighting back against insurance companies and those who have harmed others as a result of their negligence.
If youve been injured by or as a result of using a Medtronic Insulin Pump, you may be entitled to file a claim for compensation. Since its inception, our firm has won clients over $400 million in settlements and compensation.
Let us fight for you and your family. Consultations are always free and you only pay if/when we are able to achieve a verdict or settlement in your favor.
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Contact A Medtronic Minimed Insulin Pump Lawyer Today
For over 25 years, the team atZimmerman & Frachtman has been providing personalized attention to each client. We are dedicated to defending the injured and seeking justice on behalf of every client.
We strongly believe that the key to a successful attorney/client relationship is communication. We pride ourselves on keeping our clients informed of the progress of their cases and making ourselves available whenever necessary.
Our entire staff believes that the best results are obtained through good, old fashioned hard work. Over the past 25 years, the firms trial attorneys have recovered more than $300 million in verdicts and settlements on behalf of our clients. While we are quite proud of our past accomplishments, we remain true to the ideals of compassion, tenacity, consistency, discipline, and respect for others.
Fda: Medtronic Slow To Update Recall Defective Insulin Pumps For Diabetes Patients
While the U.S. Food and Drug Administration acknowledges Medtronic is actively working on fixing issues within its diabetes business, especially in regard to some of its insulin pumps, it says the steps took too long and are not enough.
Medtech giant Medtronic took more than three years to replace and start recalling insulin pumps with defective retainer rings after first becoming aware of the problem, according to an FDA warning letter sent to the company in December and recently made public.
The company also failed to investigate more than 800 complaints about defective updated retainer rings from diabetes patients who were using the product. It also failed to promptly notify the FDA within 30 days after discovering that issues with the device could lead to serious injury or death.
“In summary, your corrective actions are still in process, and you have not yet conducted effectiveness checks to ensure the updated procedures and required employee training will prevent reoccurrence of the identified deficiencies,” the FDA said in the letter.
The company did not dispute any details in the FDA’s warning letter but made the case that it is making necessary improvements in its diabetes business.
While FDA warning letters are relatively common, one expert said the recent one to Medtronic raises very serious concerns.
The FDA letter adds that Medtronic did not adequately assess the serious risk to patients of the medical device failures.
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Seven Plaintiffs File Medtronic Minimed Insulin Pump Lawsuits
A group of seven plaintiffs recently filed a new Medtronic MiniMed lawsuit in the Superior Court of California. The plaintiffs claimed that after using Medtronics 600 series insulin pumps, intended for the treatment of type 1 diabetes, they suffered serious injuries. This case was later removed to the U.S. District Court for the Central District of California.
On Nov. 21, 2019, the U.S. Food and Drug Administration announced a Class 1 recallthe most serious type of recallfor over 300,000 Medtronic MiniMed 600 series insulin pumps. The specified pumps could have a missing or broken retainer ring, which could cause under- or over-delivery of insulin, increasing the risk of injuries including hypoglycemia and hyperglycemia.
What Is The Medtronic Minimed Insulin Pump
Medtronic, a medical device manufacturer, developed the MiniMed insulin pump to combat diabetes.
An insulin pump is a small electronic device that can be easily carried on a belt or inside a pocket.
The device is attached to your body via a thin tube called an infusion set, through which insulin is delivered.
An insulin pump replaces the need for frequent injections by delivering rapid-acting insulin continuously 24 a day.
The pump and tubing can easily disconnect and reconnect to your body whenever you want to.
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Medtronic Insulin Pumps Affected By The Recall Include:
- MiniMed 600 Series Insulin Pumps
- Model 630G all lots before October 2019
- Model 670G all lots before August 2019
More than 300,000 Medtronic insulin pumps have been recalled in the United States.
According to a statement by the FDA, more than 26,000 complaints have been filed concerning this potential malfunction. Medtronic has received reports of more than 2,100 injuries and one death potentially linked to the defective product.
Losses Related To The Death Of A Loved One
When an insulin pump malfunctions, the side effects could include death. Losing a loved one through a way that could be avoided through caution, you can recover the losses related to the death of your loved one. This could include the financial support provided by the deceased or even loss of affection, companionship, and emotional support.
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Medtronic Initiated A Large
In 2017, Medtronic initiated a large-scale recall of its insulin pumps. Like prior recalls, the issue behind this recall was the over-delivery of insulin. This specific problem involved over-delivery after an infusion set change. If fluid comes into contact with the insulin reservoir, it can cause a blocked membrane. This disrupts the continuous delivery of the insulin and can cause an excess of insulin to be delivered at times. The recall was intended to change the membrane to keep fluid from coming into contact with it during an infusion set change.
The over-delivery of insulin can cause hypoglycemia, which is low blood sugar. In a worst-case scenario, this can cause death. In one instance, a man in Mississippi has claimed that his wife died after her Medtronic insulin pump administered too much insulin while she was asleep. In another instance, a New Jersey estate claimed that a man died while using a Medtronic insulin pump since the pump did not give him enough insulin.
Medtronic Recalls Over 300000 Minimed 600 Series Insulin Pumps
In November 2019, Medtronic recalled over 300,000 of its MiniMed 600 Series Insulin Pumps because of a manufacturing problem. The affected pumps could have a missing or broken retainer ring that helps lock the insulin cartridge into place in the pumps reservoir compartment. If the cartridge is not locked firmly in place, the pump may over- or under-deliver insulin, resulting in hypoglycemia or hyperglycemia . Severe hyperglycemia can result in a loss of consciousness, seizure, and death.
At the time, Medtronic was aware of 26,421 complaints in which the device malfunctioned this way, including 2175 reports of injuries and one death. Customers were advised to examine the retainer ring on their pump, and to stop using the pump if the retainer ring was loose, damaged, or missing, or if the reservoir did not lock into the pump as it should.
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History Of Class I Recalls
In August 2018, Medtronic issued a Class I Recall of its MiniMed 508 and Paradigm insulin pumps because of a cybersecurity risk involving the devices remote control.
In November 2019, Medtronic issued a Class I Recall concerning its MiniMed 600 series with an updated retainer ring.
MiniMed 600 series Insulin pump
The FDAs December 9, 2021 letter, the agency discussed:
The FDA is also beginning to enforce many corrective actions correlated with their observations during their July inspection.
Sean Salmon, the President of Medtronics Diabetes Business, stated that the company is committed to fully resolving all observations as effectively and quickly as possible.
Learn More Aboutmedtronic Minimed Lawsuits
Recalled Medtronic MiniMed insulin pumps have been linked to reports of hypoglycemia, hyperglycemia and other serious injuries.
The lawsuit indicates she was driven into a diabetic coma and when she awakened, discovered her vision was impaired, her movement uncoordinated and she had bruising and injuries indicative of having undergone diabetic seizures. She was later also diagnosed with rhabdomyolysis, orthopedic injuries, neurological damage and post-traumatic stress disorder, which resulted from the Medtronic MiniMed insulin pump failure.
Schwartz later discovered that the infusion set she had used with the device had been recalled in December 2016. The set was recalled again in September 2017, several months after Schwartzs injuries occurred. Two years later, in November 2019, a Medtronic MiniMed pump recall was issued for the actual device, after thousands of similar reports involving problems
Medtronic sent to customers in November 2019, after discovering that certain pumps may have a missing or broken retainer ring, which could result in the over or under delivery of insulin. The FDA later declared the Medtronic letter to be a Class I medical device recall, which is the most serious recall classification, and indicates that problems with a device could result in serious injury or death.
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Potential Side Effects Of The Medtronic Mini
We expect drug and medical device manufacturers to test for safety and effectiveness before putting them on the market. However, this is not always the case. Some injuries caused by defective insulin pumps can be life-altering and leave you and your family under huge medical bills. In some cases, one could lose their life from these effects. Some of the potential side effects of faulty Medtronic Mini-Med Insulin Pump include:
What Happens If The Ring On The Medtronic Minimed Insulin Pumps Is Broken
The problem is that users do not know that the small ring is broken so they continue to use and trust the pump. Two major consequences have been seen with a broken retainer ring and a malfunctioning pump.
First, too much insulin may be given to the user. Excess amounts of insulin can cause blood sugar to drop to dangerously low levels. Some of the symptoms of too much insulin are:
- An irregular or fast heartbeat
This can also lead to coma and death if treatment is not received quickly.
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An Insulin Pump Lawsuit Lawyers Team Can Review Your Case
If you or someone you loved was harmed by a recalled Medtronic insulin pump, an insulin pump lawsuit lawyer can help you. You can get a free case review from a lawyers office to learn more. Fill out our online contact form to connect with a lawyer in our network.
Get The Representation You Deserve
Standing up for those who have been injured is what we do. We give a voice to the unheard, and provide the resources needed to fight back against big insurance companies, medical device manufacturers and more.
Let us fight for you and your family. If you have been injured by the use of a Medtronic Insulin Pump, you may qualify to seek compensation.
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The Fdas Stance On The Recall
As a regulator of medical device manufacturers, this federal entity is responsible for the approval and oversight of medical devices ranging from artificial hearts and pacemakers, to stethoscopes and insulin pumps.
The U.S. Food and Drug Administration has classified the Medtronic recall as a Class I recall, the highest and most serious classification, indicating that use of the device may result in serious injury up to and including death.
According to the FDA, a Class I recall represents a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or even death.
Who Qualifies To File A Claim
Anyone who has used a Medtronic Insulin Pump that has been recalled may qualify to file a claim. Similarly, anyone who has used these insulin pumps and has experienced side effects or injuries as a result, may be eligible.
Side Effects You May Have Experienced Include:
- Increased hunger and weight gain
- Hypoglycemic episodes
- Injury from a slip or fall due to loss of consciousness or feeling lightheaded
- Brain injury
- Cardiac events
- And more
If you or a loved one have used a Medtronic Insulin Pump affected by the recalls and have experienced negative side effects, injury or death, reach out to us today. Our talented personal injury attorneys are committed to helping you get the justice and compensation you deserve.
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Medtronic Insulin Pump Lawsuit Lawyer
Medtronic insulin pump lawsuits are being filed as information comes to light about defects in Medtronic MiniMed Insulin Pumps. Our Medtronic insulin pump lawsuit attorneys are actively investigating these cases.
If you or a loved one use a Medtronic MiniMed Insulin Pump and have suffered serious injury or death, please call our experienced product liability lawyers for a FREE, no-obligation consultation.
CONSUMER ALERT: The FDA has issued a Class 1 recall for certain Medtronic insulin pumps. A Class 1 recall is the most serious type of recall, indicating that use of the potentially defective product could cause serious injury or death.
Medtronic Minimed Insulin Pump Injuries & Side Effects
As mentioned earlier, the defect in MiniMed insulin pumps was due to a fault in the retainer ring, a crucial part of the device that helps to regulate the amount of insulin administered by the pump. Because it can lead to either too little or too much insulin being administered, it means there can be two distinct types of MiniMed side effects hypoglycemia or hyperglycemia. The former refers to low levels of blood sugar, whereas the latter is high levels of blood sugar. Both conditions are dangerous and can lead to serious injury and death.
The following symptoms may be signs of hypoglycemia:
- A fruity odor/taste on your breath
- Coma and death
Please note that these are only a small selection of possible hypoglycemia and hyperglycemia symptoms that you may experience after using a faulty MiniMed insulin pump. The list is not exhaustive, and there can be some overlap between the symptoms of each condition. If you are worried, contact your doctor for advice.
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Recent Recall: Minimed 508 Paradigm Series And 600 Series Insulin Pumps
The MiniMed is popular among Type diabetes patients and recent recalls of various products have affected hundreds of thousands of Americans. If you are using one of these products, it could have a dangerous flaw. Heres what you need to know.
MiniMed 508 and MiniMed Paradigm Insulin Pump Hacking Risk
On June 27, 2019, the FDA issued a recall for all Medtronic MiniMed 508 Insulin Pump and MiniMed Paradigm Series Insulin Pumps. These specific product models were found to be vulnerable to cybersecurity risks.
The MiniMed 508 and MiniMed Paradigm were designed to communicate over a wireless radio frequency to other devices like glucose sensor transmitters and blood glucose meters. A person with the right technical skills could potentially hack a nearby insulin device and change the settings that control insulin delivery, resulting in hypoglycemia, hyperglycemia, and diabetic ketoacidosis.
Medtronic is currently issuing a recall of the following device models & software versions:
- MiniMed 508 All versions
- MiniMed Paradigm 511 All versions
- MiniMed Paradigm 512/712 All versions
- MiniMed Paradigm 515/715 All versions
- MiniMed Paradigm 522/722 All versions
- MiniMed Paradigm 522K/722K All versions
- MiniMed Paradigm 523/723 Version 2.4A or lower
- MiniMed Paradigm 523K/723K Version 2.4A or lower
- MiniMed Paradigm 712E All versions
- MiniMed Paradigm Veo 554CM/754CM Version 2.7A or lower
- MiniMed Paradigm Veo 554/754 Version 2.6A or lower