# FDA recall Z-1129-2019

> **DePuy Orthopaedics, Inc.** · Class II · device recall initiated 2018-09-21.

## Product

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.

## Reason for recall

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

## Distribution

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.

## Key facts

- **Recall number:** Z-1129-2019
- **Recalling firm:** DePuy Orthopaedics, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-09-21
- **Report date:** 2019-04-17
- **Termination date:** 2020-04-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1129-2019

## Citation

> AI Analytics. FDA recall Z-1129-2019. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-1129-2019. Source: US FDA. Licensed CC0.

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