Stryker Class 2 Recall - TrackMy® Solutions
Stryker issued a Class 2 Device Recall of its Tritanium Posterior Lumbar cage in November/December of 2018. This device originally received clearance from the FDA in November of 2015. Stryker’s reason for the recall is listed as: “The surgical technique is being updated to caution against misue due to reports of cage fractures occurring intraoperatively...
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