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Surgical Staples Litigation

The U.S. Food and Drug Administration recently issued a significant letter to health care providers about the safe use of surgical staplers and staples for internal use.

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Boston Scientific Guidewire

Atherosclerosis is a medical condition that causes hardening and the narrowing of the arteries in the body. When it affects the heart, the condition is known as coronary artery disease, which affects millions of people each year and is the number one killer of Americans.

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DePuy Synthes Distraction System

In the interest of helping patients with mandibular defects, the DePuy Synthes Craniomaxillofacial Distraction System is an implant designed to lengthen and/or stabilize the lower jawbone.

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Harbor Freight Jack Stand

Jack stands are used to safely support the weight of a vehicle while work is being performed, but if a jack stand fails injury or death can possibly occur to a person when they are defectively designed or defectively manufactured. Two different jack stand models sold by Harbor Freight have been recalled.

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Medtronic Diabetes Infusion Sets

Medtronic announced a voluntary recall of specific lots of their Diabetes Infusion Sets used with all models of Medtronic insulin pumps.

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MindFrameCapture LP Revascularization Devices

The FDA recently issued a Class 1 FDA recall (the most serious FDA recall), of several lots of MindFrameCapture LP Revascularization Devices due to a potentially lethal defect.

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Tobacco Lawsuit

With a powerful team of tobacco lawyers on your team, big tobacco can no longer avoid their responsibility for causing injury to people who use their addictive products.

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Modular Shoulder System Lawsuit

Some 50,000 shoulder replacement surgeries are done every year in the U.S. It is often recommended for those who are experiencing severe pain or stiffness due to arthritis or degenerative joint diseases.

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Zimmer Shoulder Recall

Zimmer Biomet recalled these devices because they were fracturing at higher rate than the company had stated in its labeling.

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Penumbra JET 7 Catheter Recall Litigation

The FDA has issued an important voluntary recall of the Jet 7 Xtra Flex and the Jet 7MAX catheters from Penumbra. If you or a loved one has suffered from injury due to these devices, Meyers & Flowers can help.

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