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The FDA Issues Class 1 Recall for Stryker’s Oasys Midline Occiput Plate Due to a Key Defect, Reports Parker Waichman LLP
Date:9/4/2013

caused by defective drugs or medical devices.

In the FDA’s initial recall announcement of the product, issued on May 30, 2013, it noted that the Oasys Midline Occiput Plate is part of the Oasys System, which is used in spinal surgery to promote fusion and provide stabilization at the junction between the occipital bone and the vertebrae in the cervical and thoracic spine.

On July 22, the Australian Government’s Department of Health and Ageing issued a hazard alert regarding the Oasys Midline Occipital Plate.

Parker Waichman LLP continues to offer free legal consultations to victims of injuries caused by defective medical devices. If you or a loved one experience an injury or health problem associated with a defective medical device, please contact their office by visiting the firm's Defective Medical Devices page at yourlawyer.com. Free case evaluations are also available by calling 1-800-LAW-INFO (1-800-529-4636).

Contact:
Parker Waichman LLP
Gary Falkowitz, Managing Attorney
1-(800) LAW-INFO
1-(800) 529-4636
http://www.yourlawyer.com

Read the full story at http://www.prweb.com/releases/Stryker_Oasys_recall/09/prweb11089530.htm.


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