Stryker Spine: Class I Recall
MedSun: Newsletter #88, September 2013
FDA MedWatch Safety Alert
Recall due to reports of fracture of the pin that connects the implant's tulip head to the plate body. If a patient begins experiencing symptoms including pain, weakness, or numbness, urgent evaluation is needed. For patients who have had a revision surgery, Stryker recommends routine post-operative care and follow-up.
Stryker Spine: Class I Recall. MedWatch Safety Alert. August 29, 2013.