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FDA Issues Class 1 Recall of Stryker OASYS Midline Occiput Plate Used in Spinal Surgery

By Burg Simpson

On August 29, 2013, Stryker issued a recall of a device used in spinal surgery and the FDA designated the recall as a Class 1 recall, warning that the device failure could result in serious injury or death. At issue is the OASYS Midline Occiput Plate, which is part of the OASYS Occipito Cervico Thoracic… Read more »

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