Defective Drugs

Consumers buy millions of pharmaceuticals and supplements each year safely without incident. To sustain this level of safety in the marketplace, manufacturers of drugs and supplements are held responsible for the sale of defective products that result in injury. This responsibility is broad and includes the duty to exercise reasonable care in the design and manufacture of a product. The obligation of the manufacturer to make a safe product includes the duty to design, manufacture, inspect and label a product appropriately. Proving that a manufacturer of a drug supplement is responsible for a defective product can be complicated and expensive.

Cappolino Dodd Krebs LLP utilizes personnel and experts who have specialized knowledge regarding the manufacture of defective drugs and supplements. To research whether a drug or supplement is defective requires extensive research and the resources of legal teams litigating through multiple court proceedings. If you are injured by a defective drug or supplement, save the product and all parts and instructions at the time of purchase, including the original packaging of the drug or supplement. Keep detailed notes of your condition and any other related medical records for attorneys to determine whether or not there is a viable claim against the drug manufacturer. If you have taken a defective drug, contact our firm today.

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