# FDA recall Z-1692-2020

> **Encore Medical, LP** · Class II · device recall initiated 2018-07-10.

## Product

djosurgical Linear Neck Trials with Spring Sides, Standard, nonsterile, REF S-200635; and djosurgical Linear Neck Trials with Spring Sides, Lateral, nonsterile, REF S-200636.  The firm name on the label is djosurgical, Austin, TX.

## Reason for recall

The retaining ring on the neck trials has a potential to fail interoperatively.

## Distribution

Distribution was made to CA, CO, MD, MN, OH, TX, and WA.  There was no foreign/military/government distribution.

## Key facts

- **Recall number:** Z-1692-2020
- **Recalling firm:** Encore Medical, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2018-07-10
- **Report date:** 2020-04-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Austin, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1692-2020

## Citation

> AI Analytics. FDA recall Z-1692-2020. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-1692-2020. Source: US FDA. Licensed CC0.

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