# FDA recall Z-2619-2017

> **DePuy Mitek, Inc., a Johnson & Johnson Co.** · Class II · device recall initiated 2017-05-12.

## Product

DePuy Mitek LATARJET EXPERIENCE Extraction Driver  Product Code:  288216  Product Usage:  The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft

## Reason for recall

Combo Screw Driver (Product Code 288211) tip has the increased potential to break intra-operatively when being used at an angle off-axis to screw

## Distribution

US: AZ, CA, CO, GA, MA, MI, OH, WA  Foreign:  Austria,  Australia, Belgium, France, Germany, Spain, Switzerland, Netherlands, Poland, UK

## Key facts

- **Recall number:** Z-2619-2017
- **Recalling firm:** DePuy Mitek, Inc., a Johnson & Johnson Co.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-12
- **Report date:** 2017-06-28
- **Termination date:** 2018-10-03

- **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-2619-2017

## Citation

> AI Analytics. FDA recall Z-2619-2017. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2619-2017. Source: US FDA. Licensed CC0.

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