# FDA recall Z-3210-2024

> **Stryker Spine** · Class II · device recall initiated 2024-08-23.

## Product

AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disc disease at one level from the C2-C3 disc to the C7-T1 disc.

## Reason for recall

Labeling Correction: Instructions For Use (IFU)-Updated electronic  Rev 5, specific language for indications for use for the United States and Canada was inadvertently removed.

## Distribution

Worldwide distribution - US Nationwide and the country of Canada.

## Key facts

- **Recall number:** Z-3210-2024
- **Recalling firm:** Stryker Spine
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-23
- **Report date:** 2024-10-02

- **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-3210-2024

## Citation

> AI Analytics. FDA recall Z-3210-2024. Retrieved 2026-07-10 from https://api.ai-analytics.org/recall/Z-3210-2024. Source: US FDA. Licensed CC0.

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