Some Welch Allyn AED 10 and MRL JumpStart defibrillators recalled due to potential defect. Talk to our lawyers if you were harmed.

The lawyers of our defective medicine and medical device unit are currently investigating possible lawsuits involving certain Welch Allyn defibrillators that may be defective and experience failure.

FDA and Welch Allen notified healthcare professionals and consumers of a nationwide Class I recall of 14,054 AED 10 and MRL JumpStart external defibrillators manufactured between October 3, 2002 and January 25, 2007.

These devices may experience low energy shock, unexpected device shutdown, and/or susceptibility to electromagnetic noise interference.

If such issues arise, it may prevent defibrillation of a patient in cardiac arrest and could lead to death.

This device is intended to treat adults in a heart attack (cardiac arrest).

The device analyzes an unconscious patient’s heart rhythm and automatically delivers an electrical shock to the heart if needed to restore a normal heart rhythm.

Class 1 recalls are the most serious type of recall and involve situations in which there is a reasonable probability that use of the product will cause serious injury or death.

Read the FDA Recall Notice

If you or a family member suffered injury after use of a Welch Allyn AED 10 or MRL JumpStart defibrillator, please complete the form below for a free legal review of your potential case. One of our lawyers will review it and a representative of our firm will be in touch shortly.

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Medical equipment maker Welch Allyn recalls AED heart attack devices
Law firm accepting injury cases from AED heart attack defibrillators

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