A product is considered defective if it there is a flaw in its design, if it was improperly manufactured, or if the manufacturer failed to provide adequate warnings or directions for its use. The manufacturer has a duty to warn of any known dangers of using a product. There is also a duty to warn of any dangers the manufacturer could have anticipated if the product were misused. This article discusses products liability lawsuits based on warning defect claims.
Because deaths from power window accidents are relatively rare, car manufacturers argue that the cost using the more expensive switches is not justified by the small number of deaths and injuries. Further, they claim that parents and caregivers are ultimately responsible for supervising their children in cars. Consumer safety groups argue that because the injuries and deaths are readily preventable, the change should be made even if the impact is not broad. Further, they claim that children can be injured even with parental supervision.
As a general rule, intermediaries (retailers, distributors, or wholesalers involved in distributing drugs and medical devices) have the same liability for a drug or medical device as the drug company that manufactured the product. Intermediaries that merely distribute the product can generally avoid liability, but distributors whose only activity involved unwrapping and rewrapping the products for sale to the retailer have been held liable. Some states have laws that prevent non-manufacturers from being held liable for injuries caused by defective products.
"Whenever I call your office, I always get answers–not guesses. If I need to talk with you, you're available and you don't seem to be in a rush."
– Melissa, Buffalo