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NON-FDA APPROVED SPINAL HARDWARE MAY HAVE BEEN USED IN PATIENTS AT BALTIMORE WASHINGTON MEDICAL CENTER (DR. RANDY DAVIS)

Recent reports have alleged that hundreds of unsuspecting patients who underwent spinal fusion surgery at Baltimore Washington Medical Center between 2007 and 2013 may have been implanted with defective spinal hardware, including spinal screws and other hardware. In particular, these reports suggest that patients of Dr. Randy Davis, a surgeon who operates at Baltimore Washington Medical Center, may have received and implanted spinal hardware manufactured by Spinal Solutions, Inc. that was not FDA approved, and therefore, potentially unsafe for patients. If you or a loved one were implanted with defective spinal hardware, and this was known by the doctors and/or hospital that utilized this equipment, you may have a medical malpractice against those persons or entities. The implantation of defective spinal hardware is well known to potentially result in additional harm to a person’s body, the need for subsequent removal and revision surgeries or other significant complications. At STSW, our lawyers have decades of experience in handling similar types of medical negligence or product liability types of cases involving defective medical/surgical equipment. Accordingly, if you or a loved one have had spinal fusion surgery at Baltimore Washington Medical Center between the years 2007 and 2013, you are urged to contact our office for a no cost consultation at 410-385-2225.

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