# FDA recall Z-1749-2018

> **DePuy Mitek, Inc., a Johnson & Johnson Co.** · Class II · device recall initiated 2017-12-22.

## Product

LATARJET EXPERIENCE Sharp Curved Ostetome    Product Usage:  The Latarjet EXPERIENCE Instability Shoulder Set is intended to provide to the orthopedic surgeon with a means of bone fixation and to assist in the management of reconstructive surgeries.

## Reason for recall

Reports of product loosening or coming unscrewed from the handle.

## Distribution

US Nationwide Distribution in the states of OH, WA, CO

## Key facts

- **Recall number:** Z-1749-2018
- **Recalling firm:** DePuy Mitek, Inc., a Johnson & Johnson Co.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-22
- **Report date:** 2018-05-16
- **Termination date:** 2019-07-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Raynham, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1749-2018

## Citation

> AI Analytics. FDA recall Z-1749-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1749-2018. Source: US FDA. Licensed CC0.

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