# FDA recall Z-0593-2018

> **DePuy Orthopaedics, Inc.** · Class II · device recall initiated 2017-07-12.

## Product

CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9

## Reason for recall

Incorrect device in the package. A package that was labeled as the CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9 (Part No. 3L93709 / Lot No. 5291990), contained the CORAIL HIGH OFFSET STEM Collarless SIZE 14 (Part No. L20314 / Lot No. 5292130).

## Distribution

Nationally; US Consignees for this recall are the affected are US Distributors and US Medical Facilities (Hospitals/User Facilities) that may have purchased, used, or received the affected device.

## Key facts

- **Recall number:** Z-0593-2018
- **Recalling firm:** DePuy Orthopaedics, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-07-12
- **Report date:** 2018-02-21
- **Termination date:** 2019-05-20

- **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-0593-2018

## Citation

> AI Analytics. FDA recall Z-0593-2018. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0593-2018. Source: US FDA. Licensed CC0.

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