Reported Apr 17, 2019 · Terminated

CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are…

DePuy Orthopaedics, 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: DePuy Orthopaedics, Inc. · 700 Orthopaedic Dr · Warsaw, IN · 46582-3994

Is this the product you have?

  • CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro
  • Code L20431 Product UsageThe affected CORAIL Neck Trials are surgical instruments used in CORAIL total and partial hip arthroplasty
Lot codes and dates
  • lots

    125 of 125 codes

    • 1212901
    • 1218481
    • 1226220
    • 1230761
    • 1230762
    • 1700575
    • 1781381
    • 1812714
    • 1817780
    • 1860264
    • 1865892
    • 1874689
    • 1874692
    • 1874695
    • 1885306
    • 1899212
    • 1899213
    • 1910187
    • 1979239
    • 2002010
    • 2024019
    • 2043428
    • 2043428
    • 2078239
    • 2078239
    • 2102693
    • 2102693
    • 2129111
    • 2129111
    • 2153317
    • 2153317
    • 2153318
    • 2153318
    • 2153319
    • 2153319
    • 2153320
    • 2153320
    • 2163174
    • 2163174
    • 2249115
    • 2249116
    • 2252364
    • 2274452
    • 2275487
    • 2284306
    • 2284307
    • 2309644
    • 2309645
    • 2309646
    • 2336389
    • 2336390
    • 2362086
    • 2362087
    • 2380243
    • 2384473
    • 2384474
    • 2386339
    • 2401664
    • 2401665
    • 2416615
Amount recalled
12639 total

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

There is the potential for debris/material to be found behind the O-rings in the neck trials.

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

Want the full recall guide?

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 Apr 22, 2020 · Data as of Sep 19, 5:28 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.