# FDA recall Z-0092-2019

> **Stryker Spine** · Class II · device recall initiated 2018-08-13.

## Product

AVS Aria Cage, Catalog Number 48753212    Product Usage:  The Stryker Spine AVS¿ ARIA 1M PEEK Spacers are intervertebral body fusion devices indicated for use with autogenous bone graft in patients with degenerative disc disease (DDD) at one level or two contiguous levels from L2 to S1 . The AVS¿ ARIA TM PEEK Spacers are intended to be used with supplemental fixation systems that have been cleared for use in the lumbosacral spine.

## Reason for recall

The anterior and posterior markers on the cage were on the incorrect/opposite sides of the cage.

## Distribution

US Nationwide in the states:  CA, FL, GA, MI, MN, NJ, NM, and OR

## Key facts

- **Recall number:** Z-0092-2019
- **Recalling firm:** Stryker Spine
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-08-13
- **Report date:** 2018-10-17
- **Termination date:** 2019-05-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Allendale, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0092-2019

## Citation

> AI Analytics. FDA recall Z-0092-2019. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-0092-2019. Source: US FDA. Licensed CC0.

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