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Product Liability

FDA Requests Removal of Zantac

The U.S. Food and Drug Administration (FDA) recently requested that manufacturers immediately withdraw all prescription and over-the-counter (OTC) ranitidine – commonly known by the brand name Zantac – from the market. This move is the latest in...

Pelvic Mesh Malfunctions

Thousands of vaginal pelvic mesh implant procedures are performed each year across the United States.  Surgical vaginal pelvic mesh implant procedures are used in women in order to repair the structures that support the bladder, uterus, and bowel w...

Stryker Hip Product Recall

Recently, the medical technology company, Stryker, announced a recall of its Rejuvenate Modular Necks and ABG II Modular-Neck stem implants, as well as the LFIT V40 Model. The recall was issued after the devices were linked to high rates of fretting...

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