Reported Apr 17, 2019 · Terminated

CORAIL AMT HIGH OFFSET NECK SEGMENT (KHO), Pro. Code L20433 Product Usage: The affected CORAIL Neck Trials are surgical…

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 HIGH OFFSET NECK SEGMENT (KHO), Pro
  • Code L20433 Product UsageThe affected CORAIL Neck Trials are surgical instruments used in CORAIL total and partial hip arthroplasty
Lot codes and dates
  • 121 of 121 codes

    • 1216681
    • 1216682
    • 1230767
    • 1230768
    • 1230769
    • 1700574
    • 1700577
    • 1781383
    • 1812717
    • 1817782
    • 1860266
    • 1865894
    • 1874691
    • 1874694
    • 1874697
    • 1885308
    • 1899216
    • 1899217
    • 1910189
    • 2002012
    • 2024021
    • 2043430
    • 2043430
    • 2065508
    • 2065508
    • 2078241
    • 2078241
    • 2102703
    • 2102703
    • 2102704
    • 2102704
    • 2129113
    • 2129113
    • 2142423
    • 2142423
    • 2153325
    • 2153325
    • 2153326
    • 2153326
    • 2173203
    • 2173203
    • 2249175
    • 2249176
    • 2249177
    • 2252365
    • 2274507
    • 2284309
    • 2284310
    • 2309652
    • 2309653
    • 2309654
    • 2336394
    • 2336395
    • 2362088
    • 2362089
    • 2380244
    • 2384477
    • 2384478
    • 2401667
    • 2416621
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, 4:53 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.