DePuy Orthopaedics, Inc.: Medical Device Recalls in 2019

Updated on March 25, 2026.

According to to data from the FDA, there were 3 medical device recalls made by DePuy Orthopaedics, Inc. in 2019. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

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.
CORAIL AMT HIGH OFFSET NECK SEGMENT (KHO), Pro. Code L20433 Product Usage: The affected CORAIL Neck Trials are surgical instruments used in CORAIL total and partial hip arthroplasty.
CORAIL AMT COXA VARA NECK SEGMENT (KLA) Pro. Code L20432 Product Usage: The affected CORAIL Neck Trials are surgical instruments used in CORAIL total and partial hip arthroplasty.