DePuy Orthopaedics, Inc. recalls CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are s

Recalled April 17, 2019 · FDA recall Z-1127-2019 · DePuy Orthopaedics

Hazard

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

Units

12639 total

Sold at

Worldwide Distribution - US Nationwide Distributed to accounts in AL AZ CA CO FL GA HI IA IL IN KY LA MA MD ME MI MN MS NC ND NH NJ NV NY OH OR PA SC TN TX UT VA WA, and WI. International distribution worldwide.

Description

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

Product

CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD), Pro. Code L20431 Product Usage: The affected CORAIL Neck Trials are surgical instruments used in CORAIL total and partial hip arthroplasty.

Manufacturer(s)

DePuy Orthopaedics, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →