Reported Nov 4, 2015 · Terminated

Exprt Precision System: Revision Knee, Model Number 160-010-726/738 For use with the Exprt Knee System in total knee…

Encore Medical, LP

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: Encore Medical, Lp · 9800 Metric Blvd · Austin, TX · 78758-5445

Is this the product you have?

  • Exprt Precision SystemRevision Knee, Model Number 160-010-726/738 For use with the Exprt Knee System in total knee arthroplasty to replace the native patella
Lot codes and dates

5 of 5 products · 5 lot codes

Recalled lot codes, grouped by product number
Product numberLot codes and dates
471T1-001
  • 011
472T1-000
  • 014
473T1-000
  • 015
474T1-000
  • 010
475T1-000
  • 008
Amount recalled
209 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

The labeling is missing the size/diameter information.

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

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Jan 4, 2016 · Data as of Sep 19, 6:00 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.