# FDA recall Z-1750-2018

> **Medtronic Sofamor Danek USA Inc** · Class II · device recall initiated 2018-03-23.

## Product

Medtronic ZEVO(TM) Anterior Cervical Plate System SLOT SCREW, REF 7710015, Size 4.5mm x 15mm    Product Appliance, fixation, spinal intervertebral body

## Reason for recall

Slot screw had an overall length of 15mm, but per the specification, the screw should have an overall length of approximately 17mm.

## Distribution

Worldwide Distribution - US Nationwide in the states of GA, CT, LA, MD, WY, IN, MD, FL, and France

## Key facts

- **Recall number:** Z-1750-2018
- **Recalling firm:** Medtronic Sofamor Danek USA Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-03-23
- **Report date:** 2018-05-16
- **Termination date:** 2021-07-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Memphis, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1750-2018

## Citation

> AI Analytics. FDA recall Z-1750-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-1750-2018. Source: US FDA. Licensed CC0.

---

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