# FDA recall Z-1426-2026

> **Centinel Spine, Inc.** · Class II · device recall initiated 2025-12-31.

## Product

Brand Name: Prodisc  Product Name: Prodisc C SK  Model/Catalog Number: PDSL6  Software Version: N/A  Product Description: Total cervical disc replacement  Component: No

## Reason for recall

Products were mislabeled as the 6mm product but included the 5 mm product.

## Distribution

US Nationwide distribution in the states of AL, CA, CO, LA, NY, OR, TN, TX.

## Key facts

- **Recall number:** Z-1426-2026
- **Recalling firm:** Centinel Spine, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-31
- **Report date:** 2026-02-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** West Chester, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1426-2026

## Citation

> AI Analytics. FDA recall Z-1426-2026. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1426-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*