Recalled Drug Lawyers in Ohio

We rely on pharmaceutical companies to develop drugs and medical devices that help us control and treat medical conditions, diseases, and injuries. Sadly, sometimes these drugs and medical devices have defects that lead to serious side effects such as stroke, heart attack, kidney failure, certain types of cancer, and even death. Even if these dangerous drugs are recalled, you can still suffer from their side effects and be left with medical bills, lost wages, and a great deal of pain and suffering.

If you’ve been hurt by a recalled drug, it is in your best interest to consult the experienced Ohio product liability attorneys at Kisling, Nestico & Redick by calling 1-800-HURT-NOW. We have years of experience representing clients in drug recall cases and will help you recover compensation for your damages.

Responsibilities of Pharmaceutical Companies in Ohio

Pharmaceutical companies are responsible for testing their drugs and medical devices prior to submitting them for approval by the Food and Drug Administration (FDA). These companies must also ensure that the labels on their drugs and medical devices include any side effects and warnings so that doctors and consumers are aware of any risks. If pharmaceutical companies fail to adhere to these requirements and a design defect, manufacturing flaw, or insufficient labels/warnings are found, they can be held liable in a product liability lawsuit.

How Drug Recalls Work in Ohio

A drug recall begins when there are reports from doctors, patients, pharmaceutical companies, or any group or individual that discovered a problem with the drug or medical device. Once there have been reports of unsafe drugs or devices, these goods will be assessed for danger. Details about the issues these drugs and devices cause will be evaluated to determine if the reports are valid. In the event that the reports are, indeed, valid, the recall must be reported to the United States Department of Health within 24 hours.

Since each recall is different, the strategy of recalling hazardous drugs or medical devices will depend on how dangerous the drug is, and whether a level I, II, or III recall will be issued. After the strategy has been designed, information about the recall will be published on the FDA’s website, and the FDA will monitor the recall to make sure it is implemented properly. Details regarding the recalled drug or device will be available to the public via the archives on the FDA website.