Stryker Class 2 Recall

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 and postoperatively.”

The recall was initiated on November 28th of 2018. The FDA is currently investigating the cause of the recall.

If you have this device please contact your Surgeon and then signup for our medical device recall tracking service, TrackMy Implants. It is free and keeps you notified in real-time. Read more about us.