Reported Sep 18, 2019 · Terminated

Vanguard XP Tibial Tray 79 mm Item # 195252

Zimmer Biomet, 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: Zimmer Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989

Is this the product you have?

  • Vanguard XP Tibial Tray 79 mm Item # 195252
Lot codes and dates
  • Lot Number
    • 332750
    • 833230
    • 515120
    • 752550
    • 515130
    • 373090
    • 919280
    • 754510
    • 764430
    • 764440
    • 861230
    • 837810
    • 846560
    • 907730
    • 928810
    • 907720
    • 907740
    • 969000
    • 969010
    • 590620
    • 590600
    • 663320
    • 663330
    • 663340
    • 590610
    • 571010
    • 663310
Amount recalled
99 units

This recall covers 35 products

The agency filed one notice per product. You are reading one of them; the other 34 are below.

22 more are in the archive.

Where it was sold

Why it was recalled

The locking bar not fully engaging

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 Apr 16, 2021 · Data as of Sep 19, 5:34 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.