# FDA recall Z-1773-2026

> **XTANT Medical Holdings, Inc** · Class II · device recall initiated 2026-02-18.

## Product

XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL.

## Reason for recall

Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.

## Distribution

US:  OR

## Key facts

- **Recall number:** Z-1773-2026
- **Recalling firm:** XTANT Medical Holdings, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-02-18
- **Report date:** 2026-04-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Belgrade, MT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1773-2026

## Citation

> AI Analytics. FDA recall Z-1773-2026. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1773-2026. Source: US FDA. Licensed CC0.

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