---
title: "XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number ... — FDA record Z-1773-2026 | Is It on Recall"
description: "Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is."
url: https://isitonrecall.com/recall/fda-device-z-1773-2026-xtant-medical-xpress-pedicle-screw-system-dual-lead-6-5-x-50-mm-part-number-x073-6555-dl/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL. — FDA record Z-1773-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Feb 18, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL.
- **Reason**: Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.
- **Classification**: Class II
- **Recalling firm**: XTANT Medical Holdings, Inc
- **Quantity**: 2 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1773-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1773-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI/DI M697X0736555DL1, Lot Number 4375-01 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: OR

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Oregon](https://isitonrecall.com/state/oregon/)

## Dates in the source

- **Report date**: Apr 15, 2026
- **Recall initiation date**: Feb 18, 2026
- **Center classification date**: Apr 3, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1773-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [XTANT Medical Holdings, Inc records](https://isitonrecall.com/brand/xtant-medical-holdings-inc/)