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Recall Observatory FDA recall evidence

Device product

Irix-A Integrated Lumbar Fusion System, Model Number X080-423011-08PC (Spacer Assy, 42 X 30 X 8¿, 11mm, PC (STERILE)) and Model Number X080-382819-08PC (Spacer ASSY, 38 X 28 X 8¿, 19mm, PC, (STERILE))

Z-1177-2025

January 03, 2025

Class II

Product summary

Firm
XTANT Medical Holdings, Inc
Event
Event 96179
Status
Ongoing
Classification
Class II
Quantity
14 units
Official record key
device-enforcement:Z-1177-2025

Official wording

Reason: Certain implants in the Irix-A Lumbar Fusion System were distributed while labeled with an incorrect expiration date.

Code information: Model X080-382819-08PC-STR: UDI-DI M697X08038281908PCSTR1, Lot Number 054961; Model Number X080-423011-08PC-STR: UDI-DI: M697X08042301108PCSTR1, Lot Number 053028

Distribution pattern: Worldwide - US Nationwide distribution in the states of AZ, CA, CO, LA, OH, TX, and WV. The country of Australia.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Certain implants in the Irix-A Lumbar Fusion System were distributed while labeled with an incorrect expiration date.