Class I Recall for Stryker’s OASYS Midline Occiput Plate

On August 29, 2013, the FDA and Stryker notified healthcare providers of a class I recall of Stryker’s OASYS Midline Occiput Plate.  This most serious type of recall was issued because of reports of fracture of the pin that connects the implant's head to the plate body. According to their website, Stryker is one of the world’s [...]