Medical device manufacturer Stryker has recalled units of its LIFEPAK 15 Monitor/Defibrillators after it was discovered the device could lock up during use. 
According to the Atlanta Journal Constitution, the recall announcement was made by the U.S. Food and Drug Administration (FDA). It was reported that the device could potentially lock up if a defibrillation shock is delivered to a person.
Stryker is supposed to notify affected customers if their devices are involved in the recall. During the malfunction, the device reportedly illuminates lights indicating that it is still on, but there is no response or function.
According to the FDA, since 2009, there have been a reported six deaths and 58 complaints globally linked to the device. It is estimated that 13,000 devices will be impacted by the recall.
“The company is instructing customers to continue to use their LIFEPAK 15 Monitor/Defibrillator according to the Operating Instructions until the correction can be completed,” the FDA press release said.
To view the press release, you can click on the source link below.
Can You Hold a Defective Medical Device Manufacturer Liable for Injuries?
Defective medical device manufacturers must be held liable when they injure or kill someone.
It is sad that these defibrillator malfunctions can be tracked to deaths. If you or a loved one has been injured by a faulty medical device, contact our Texas personal injury attorneys at for a no-cost consultation.
Medical device manufacturers have a duty to test products and make sure they are safe before they are marketed to the public.
We hold defective product manufacturers liable—we are the personal injury law experts of Central Texas.
