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zimmer knee implant recallZimmer voluntarily started recalling their Persona Trabecular Metal Tibial Plate knee replacement system in March. The Federal Drug Administration (FDA) issued a Class II recall for all makes and sizes. Companies are responsible for providing product liability for any product they produce and sell.

The FDA Class II Recalls are an intermediate level of concern. There is no immediate danger of death or serious injury, but there is still a possibility if the product’s use is continued. There are also still health and safety concerns. The FDA works with the manufacturer to help patients affected by the product recall to ensure the product is taken off the market as soon as possible.

In the case of Zimmer, they started recalling their Persona Trabecular Metal Tibial Plate system on their own, but not fast enough for the FDA. Complaints started increasing concerning implants loosening and causing complications. Over 11,500 devices are affected by the recall. The Persona system is not the first recall Zimmer has experienced. Two other products they have produced in the past have recently been recalled and taken off the market for similar complaints of the devices loosening. How can a company continue to be trusted to produce products if their products continue to be recalled for similar issues among different devices?

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Chicago defective product lawyerThe Takata airbag recall has been unfolding since October, starting with a massive recall that affected 11 car companies. The Takata recall was already setting records for the amount of companies it affected with the recall. On May 19, Takata nearly doubled the recall amount and now affects approximately 34 million vehicles. It is now the largest automotive recall in history.

With the recall almost doubling, it may take years to replace the airbags that are being recalled. New processing procedures and airbags have to be produced and then shipped to dealers for replacement. Implementing a new process for producing the airbags may require modifying machines, training employees, and the other procedures to ensure their product is safe. This can take time to implement, making consumers who have to have their airbags replaced wait even longer. Takata and the car companies have a product liability responsibility to the consumer to ensure their products are safe to use.

While the National Highways Traffic Safety Administration (NHTSA) and Takata will not have all the vehicles affected for a few weeks at least, of the 11 companies affected by the recall, Honda has been affected the most. Reports have been reviewed about if Honda knew about the defects before the recall was issued and did not report it to the NHTSA, but Honda has started looking into other companies for replacing the airbags. The solution is coming a little too late for some consumers who have already been affected by the defect, including families who have lost family members due to the defective airbags.

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surgical staple recall, Chicago Illinois product liability lawyerWhen the Federal Drug Administration (FDA) issues a recall, it is classified into one of three classes: Class I, II, or III. A Class I recall is the most serious recall the FDA issues. The TigerPaw II system recall has been classified as a Class I recall and patients who have had the system used during heart surgery should immediately speak with their surgeon. Patients who have had the staples used during surgery may also want to consider contacting a product liability attorney to talk about compensation from Maquet Medical Systems, the maker of the TigerPaw II system, for a product liability case.

The TigerPaw II system is a surgical staple used to close tissue in the left atrial appendage of the heart. It has been reported to cause tearing and bleeding in the heart tissue due to not closing completely. The FDA recall affects all TigerPaw II systems, which is over 4,000 TigerPaw II systems. They recommend the staples be immediately removed, quarantined, and replaced.

When the FDA classifies a recall as a Class I it is because there is a  strong likelihood that the product will cause serious adverse health consequences or death if use of the product continues. Maquet Medical Systems received 51 reports of adverse side effects and one death associated with the TigerPaw II system between April 2013 and March 2015.

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black decker lawnmower recall, Chicago product liability attorneyWhen companies receive reports and supporting evidence of safety hazards for a product they produce, they have a 24-hour window in which they are supposed to report it to the Consumer Product Safety Commission (CPSC). Not doing so can cause other consumers using the product to injure themselves due to the defect. Black & Decker did not comply with the requirement to report the safety defect for allegedly 11 years. They have a responsibility to consumers to report safety defects immediately and compensate them for product liability.

This will be the fifth time Black & Decker has been fined for not reporting safety hazards to consumers immediately concerning their products. The company is being required to pay a $1.575 million civil penalty to settle the allegations.

The products in question this time are two electric lawn mowers. Consumers reported that the lawn mower models would turn back on after the handle was released and the safety key removed. In some cases, the lawn mower would run for hours after it had originally been turned off and it had restarted on its own. The defect in the products has caused several injuries and the company had received over 100 reports.

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bicycle recalls Chicago, Illinois product liability attorneyAccording to a recent survey by Active Times, Trek was rated the number one bike brand in 2014 because they consistently produce quality bicycles and make advancements to the industry. How will the recent recall of nearly one million Trek bicycles due to a defect in their quick release brake lever on certain bicycle models affect that rating?

With the number of cyclists increasing in recent years, cyclists want to know that the bicycle they purchase will be safe. Defective bicycle parts are a safety issue and can cause hazards not only for the cyclists, but also their family and anyone else involved in an accident caused by a defective part.

The models being recalled were manufactured from 2010 to 2015, have a silver or black quick release lever on the front wheel, and front disc brakes. The defect can cause the quick release lever to become stuck in the front disc brake causing the bicycle to stop suddenly and throw the cyclist over the front handlebars or cause the front wheel to come off. The defect has caused one cyclist to become paralyzed and injured two others.

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