Product Liability- Drugs and Recalls
Medications and drug-related products are common contributors to the high number of product liability claims brought every year. Even after receiving approval of the U.S. Food and Drug Administration (FDA) and meeting testing standards of quality control, some drugs can still have defects that contribute to the death or injury of many individuals. Numerous drugs have been recalled throughout the years, many of which once had FDA approval. These include drugs used for depression, allergies, dieting, chronic pain, and other commonly reported needs. Some drugs continue to remain on the market even after reports of dangerous side effects. A qualified New York Drug attorney can help a person decide on the proper steps to take for getting legal compensation if they become injured by a drug or prescription medication.
Manufacturer’s Duty
Drug manufacturers are required to provide warnings of potential side effects of any drug they produce. Their status as an expert in the field also makes them responsible for staying updated on the effects of their products after they have been released to the public, and taking corrective action when an issue arises.
Issues of Safety
Some drug products are put on the market with known potentially dangerous side effects if they cannot be altered for safety and still retain their benefits to users. These are often administered with sufficient warnings and in this type of case, if one sustains injuries, the odds of winning a products liability suit is typically low. Individuals should always use caution when taking any type of medication and make sure they are well informed on potential dangers or side effects.
Sorting Out the Complexities
Many elements are involved in proving product liability, and in some cases, there are multiple parties that should be held accountable. A personal injury attorney who specializes in product liability in New York & New Jersey can help sort out the complexities of individual cases.
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