FDA recall record

Smith & Nephew smith&nephew LEGION L-WEDGE, 10 MM DIS X 5 MM POS, SIZE 4, SCREW-ON FEMORAL recall — FDA Z-0092-2018

The Legion Screw-on Wedge Size 4 contained 5MM screws instead of the required 10MM screw.

Class IIclassification
Z-0092-2018official record ID
Nov 22, 2017report date

Recall record at a glance

Official recordZ-0092-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSmith & Nephew, Inc.
Report dateNov 22, 2017
Recall initiation dateSep 14, 2017
Quantity10 units
LocationMemphis, TN, United States

Official product description

smith&nephew LEGION L-WEDGE, 10 MM DIS X 5 MM POS, SIZE 4, SCREW-ON FEMORAL WEDGE, REF 71421733, STERILE R Product The Revision Knee System Components are indicated for rheumatoid arthritis; post-traumatic arthritis; osteoarthritis; degenerative arthritis; and failed osteotomies, hemiarthroplasties; unicompartmental replacement; or total knee arthroplasties. The components are designed for use in primary and revision surgery, where the posterior cruciate ligament and one or both of the collateral ligaments (i.e., medial collateral and/or lateral collateral ligament) are absent or incompetent. The Revision Knee Components are for single use only and are intended for implantation with bone cement.

Why the product was recalled

The Legion Screw-on Wedge Size 4 contained 5MM screws instead of the required 10MM screw.

Distribution information

US, Belgium, Ecuador, Netherlands, Puerto Rico, Switzerland, Thailand

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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