Product Liability – Defective Medical Device: Following a voluntary Recall in May, The FDA recently issued a Class I Recall for the OASYS Midline Occiput Plate, a spinal implant manufactured by Stryker
The defective product, the OASYS Midline Occiput Plate, is a specific part of the OASYS system which is used in spinal surgery to promote fusion and provide stabilization at the junction between the occipital bone and the vertebrae in the cervical and thoracic spine (see picture below of the plate and of the whole OASYS system installed on the spine).
According to the FDA, the pin that connects the tulip head to the plate body can break after the surgery has been performed which may cause serious adverse health consequences including blood loss, nerve injury, and the need for revision surgery to replace the fractured implant.
Class I recalls are issued by the FDA for dangerous or defective products that predictably could cause serious health problems or death.
New York Personal Injury Attorneys Blog


You won’t believe how many things can go wrong with this simple kettle: the spout is defective and water can spill posing a burn hazard, the steam can travel up to the handle and burn your hands. Additionally the leaking steam can prevent the kettle from whistling and if all the water evaporates the kettle may actually melt on your stove! 

“No helmet system can protect you from serious brain and/or neck injuries including paralysis or death. To avoid these risks, do not engage in the sport of football” is the type of language that consumers will read on most warning labels when they purchase a football helmet these days.
Millions of toys that contained dangerous levels of lead paint and other toxins as well as dangerous children products have been recalled since the Consumer Safety Improvement Act was signed into law 5 years ago.