FDA announces recall of Stryker cutting guide for TKA

Clinical Topics Musculoskeletal/Orthopedics News Web Exclusives

FDA announces recall of Stryker cutting guide for TKA

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April 11, 2013

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.

*Online Bonus Content: This has not been peer reviewed. The views and opinions expressed here are those of the author and do not necessarily reflect the opinions or recommendations of the American Nurses Association, the Editorial Advisory Board members, or the Publisher, Editors and staff of American Nurse Journal.

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