HomeClinical TopicsFDA announces recall of Stryker cutting guide for TKA

FDA announces recall of Stryker cutting guide for TKA

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On April 19, the U.S. Food and Drug Administration (FDA) announced that Stryker Orthopaedics has recalled ShapeMatch Cutting Guides, used in total knee arthroplasty (TKA) instrumentation. Read more.

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