XTANT Medical Holdings, Inc 2026-04-15 Health serious FDA
Health · FDA · Recall #FDA-Z-1773-2026
XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL. Recall
Issued April 15, 2026 · XTANT Medical Holdings, Inc
In April 2026, XTANT Medical Holdings, Inc recalled the XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL., a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.
What you should do
- 1 Stop using XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL. right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact XTANT Medical Holdings, Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- XTANT Medical Holdings, Inc
- Category
- Health
- Recall date
- April 15, 2026
- Units affected
- Not reported
- Sold at
- US: OR
- Recall number
- FDA-Z-1773-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- XTANT Medical Holdings, Inc has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.