Some side effects caused by using the recalled insulin pumps are confusion, fainting, dizziness, difficulty speaking, sweating, seizures, coma, and death. In May 2008, Medtronic also recalled their SynchroMed II insulin pumps.
Last year, the voluntary Medtronic recall involved certain lots of their Quick-set infusions used in MiniMed Paradigm insulin pumps. Forty-one of these patients suffered from diabetic coma, low blood sugar, or other problems before death. Since they rely on the insulin pump to administer medication daily, insulin pump malfunctions could have a severe effect hydraulic cylinder price on the reported 375,000 Americans using insulin pumps. These infusions are used to deliver the medication from the insulin pump to the patient. These recalls, such as the Medtronic recall last year, relate to hardware and software problems with the pumps, which have caused serious, and sometimes fatal, injuries to users.com
Bernstein Liebhard LLP has been exclusively representing injured plaintiffs in complex individual and class actions for over 15 years, recovering almost $3 billion for our clients.com) March 19, 2010 – New York, Mar 19, 2010 — The attorneys at Bernstein Liebhard LLC are disturbed by the news of the growing number of insulin pump related recalls.
Malfunctions in the infusions affected the dosage of insulin which resulted in injury and sometimes death.
A lawsuit was filed against Medtronic and some of its subsidiaries in U. Reuters reports that the FDA looked closely into 17,000 reports of insulin pump-related health problems from 2006 through 2009, and reviewed 310 fatality reports. According to The Wall Street Journal, there have been 18 insulin pump-related recalls by the FDA over the last five years. Affected infusions are MMT-396, MMT-397, MMT-399, and lot numbers starting with the number 8. For more information on the Medtronic recall and Bernstein Liebhard LLP, please visit: or call (877) 779-1414.
The hardware and software problems stretch beyond the Medtronic recall and span different manufacturers and products. District Court in the Southern District of Texas on November 30, 2009. As a result of the increasing incidence of pump malfunctions, on March 2, 2010, the FDA announced that it is convening a panel of medical experts in order to “minimize the risks associated with the devices in these recall situations. The Medtronic recall took place after the company received a letter warning that insulin pumps without propellant had been inserted in patients.”
The recalled insulin pumps are generally used by people with type 1 diabetes. The Medtronic lawsuit involves claims for damages under theories of strict liability, negligence, failure to warn, defective design and manufacturing, and breach of warranty. Some other insulin pump manufacturers involved in the recalls besides Medtronic are Roche Holding AG, and Johnson & Johnson. The Medtronic lawsuit also seeks punitive damages, claiming that Medtronic was aware of the risk of their products and production deficiencies. The firm is nationally recognized as a leader in the plaintiffs’ bar, and has been named as one of the top plaintiff’s litigation firms in the country by the National Law Journal for the last seven years.