Legal Assistance Best Criminal Fraud Lawyer Orange Cove California – When Lawyers Compete, You Win! – 844-292-1318 California legal aid

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Medical identity theft refers to fraudulent use of a person’s identity or personal health information in order to receive health care services or goods. A survey had shown that 1.84 million people were victims of medical identity theft in 2013. An estimated cost of this type of fraud made up .6 billion. Sometimes people intentionally allow to use their health insurance by uninsured persons to help them obtain medical care. This is called “Robin Hood” crimes. This type of crime constituted 30% of medical ID theft in 2013.

There are a lot of reasons to steal medical identity. Another person’s identity could help you buy addictive drugs or receive free treatment. Stolen medical ID can lead to loss of health coverage, ruined credit because of the unpaid hospital bills in your name. The thief’s treatment data included in your medical records can result in wrong treatment for you and can threaten your life or health.

In order to prevent medical identity theft it is important to monitor your health records, not to share your personal information with people you don’t know, keep copies of your health care records. Don’t forget to stay away from “free” medical services and monitor your credit reports.

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U.S. Food and Drug Administration (FDA) is the oldest consumer protection agency in the U.S. Federal Government and its regulatory functions began with the 1906 Pure Food and Drugs Act. FDA received in 1930 its present name and this organization is responsible for protecting public health in the areas such as Human and Veterinary Drugs, Biological Products, Medical Devices, Nation’s Food Supply, Cosmetics and Products that emit radiation.

The term of Product Recall is defined by U.S. Food and Drug Administration as removal of the product from the market in the cases when the company discovers problems on their own and decides to recall their own product voluntarily or the product is removed after the FDA raises concerns. When the product is defective or potentially harmful a correction could be made to it.

It is important to note, that there are different types of FDA Drug Recalls. Class I Recalls include a situation where is a reasonable probability that the use or exposure to a violative product will cause serious adverse health consequences or death. Class II Recalls include the probability of the product to cause temporary or medically reversible adverse health consequences or when the probability of serious adverse health consequences is remote. Class III Recalls represent a situation in which use or exposure to a violative product is not likely to cause adverse health consequences. Market withdrawals can occur when a product has a minor violation that would not be subject to FDA legal action. The firm itself can remove their product from the market in order to correct the violation. A medical safety alert may be issued when a medical device may present an unreasonable risk of substantial harm, these situations sometimes are considered recalls.

If you or a family member has been affected by a harmful product or drug, you should seek a qualified personal injury attorney who specializes in this area.

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