Faulty Design Causes Problem with Insulin Pump Power Pack
Insulin Pump Power Pack Recalled
WASHINGTON, DC — August 11, 2006 — The Disetronic D–TRONplus Power Pack has been recalled by its manufacturer (Press Release, July 13, 2006). The power pack operates the D–TRONplus Insulin Pump, which delivers insulin to diabetes patients. However, the device may shut down the insulin pump without any warning, stopping the receipt of insulin. This in turn may cause hyperglycemia or high blood sugar, resulting in serious injury or death.
The problem is due to a battery design change, according to the power pack manufacturer, Disetronic Medical Systems Inc. (Disetronic). The company suggests that all pump users put new power packs into their insulin pumps every two weeks to prevent their pumps from turning off without any warning. Disetronic will provide free power packs to users every two weeks until the problem with the current power pack can be fixed.
Meanwhile, doctors should carefully monitor their patients for signs of inadequate insulin delivery and hyperglycemia. Patients should also be aware of hyperglycemia symptoms, which include:
- Nausea and vomiting
- Blurred vision
- Excess thirst or hunger
- Frequent urination
- Fatigue
- Headache
- Fruity acetone breath
- Abdominal pain
Any adverse reactions from the use of the Disetronic D–TRONplus Power Pack should be reported to the FDA’s MedWatch Program by phone at 1–800–FDA–1088, or by Fax at 1–800–FDA–0178.
Brayton Purcell and Medical Device Cases
Brayton Purcell has represented hundreds of plaintiffs in medical device cases, including people injured by artificial implants, intrauterine devices and coronary surgery equipment. We will continue to fight to make manufacturers accountable to the public for defective medical devices and to protect our injured clients. If you or a member of your family has been a victim of an unsafe medical device, please contact us for a free review of your potential case.
