Dangerous Drug and Medical Device Claims

When a drug or medical device causes serious injury that patients were not warned about, the manufacturer may be responsible.

These cases are often coordinated nationally, but each injured person keeps their own claim.

Claims We Review

• Bard PowerPort and implanted port catheters: catheter fracture, migration, infection and blood clots.
• We also review claims involving: hair relaxer and uterine cancer; Suboxone film and tooth decay; Depo-Provera and meningioma; and GLP-1 drugs such as Ozempic and Wegovy and sudden vision loss (NAION).

What to Gather

• The name of the drug or device
• When you used it, or when it was implanted
• The injury and its diagnosis
• Your treating providers

For product cases that do not involve drugs or devices, see defective products.

Frequently Asked Questions

Do I need to know the exact product?

It helps, but we can often identify it from pharmacy or medical records.

Is this a class action?

Usually not. Most of these cases are individual claims coordinated with others before one judge.