Reported Mar 25, 2020 · Terminated

LEGION PS High Flex XLPE size 5-6 9mm Articular Insert

Smith & Nephew, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Smith & Nephew, Inc. · 1450 E Brooks Rd · Memphis, TN · 38116-1804

Is this the product you have?

  • LEGION PS High Flex XLPE size 5-6 9mm Articular Insert
Lot codes and dates
    • Lot Number 19FM12500
    • Product Number 71453221
Amount recalled
29 units

Where it was sold

Why it was recalled

LEGION PS High Flex XLPE Articular Insert was packaged with an incorrect part

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Sep 4, 2024 · Data as of Sep 19, 6:14 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.