For over 30 years, Harry S. Cohen & Associates has been helping those who have been injured by the negligence of hospitals and doctors. We also help people who have been harmed or killed by dangerous drugs and defective medical devices.
Drug and Device Manufactures are Responsible for Patient Safety
In the United States, drugs and medical devices must gain approval from the U.S. Food & Drug Administration (FDA) in order to be sold. However, approval does not guarantee a drug or medical device is safe. In fact, many products that were approved by the FDA and have been proven to cause significant harm and even death to patients. Some medical devices and drugs have a defect in the product, unreported side effects, incomplete labeling, or insufficient warnings that can cause physical, psychological, or emotional injury. The manufacturer of the drug or device is responsible for ensuring that its label is updated to protect the public safety.
Harry S. Cohen & Associates is committed to holding drug and device makers and marketers accountable for the harm they cause. We are currently reviewing cases against the manufacturer of the following dangerous drugs and defective products:
- Hernia Mesh
- Paragard IUD
- Breast Implants
- Talcum Powder
- 3M Ear Plugs
- Hip Replacements
- Proton Pump Inhibitors
Free Dangerous Drug or Defective Device Consultation
If you believe that you or a loved one was injured by a defective drug or product, please contact the product liability at Harry S. Cohen & Associates today at 1-800-MEDMAL1. There is no charge for an initial, confidential consultation, and there is never an out of pocket- fee for our clients.