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Medium risk Drugs & MedicationsClass II

XTANT Medical Holdings, Inc Recall

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

Updated February 18, 2026

XTANT Medical Holdings, Inc is recalling XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL.. Hazard: Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.

Is the XTANT Medical Holdings, Inc recalled? Yes. This product was recalled by FDA on February 18, 2026. Details below.

What is recalled

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

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The hazard

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

Brands affected

XTANT Medical Holdings, Inc
Source
FDA
Category
Drugs & Medications
Recall ID
fda-Z-1773-2026
Classification
Class II
Recalled
February 18, 2026
Read the official notice

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