recall

5:49 pm
Thu April 11, 2013

Recalled knee surgery tool could cause damages, death

Lead in text: 
Stryker recalled ShapeMatch Cutting Guides in November for concerns that the tool may cause the knee not to work properly.
KALAMAZOO, MI - Stryker Corp.'s voluntary recall of its ShapeMatch Cutting Guides is being classified as a Class I recall by the Food and Drug Administration, meaning there is reasonable probability the product could cause serious adverse health consequences or death.