XIA 3Recalls & reported problems across all models
Stryker Corporation · 93 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 537
- Deaths reported
- 0
- Injuries reported
- 239
- Recalls
- 0
We found 93 models of XIA 3 by Stryker Corporation in the FDA's device registry (GUDID). Together they are named in 537 adverse event reports in the FDA's MAUDE database, received between Feb 9, 2016 and Sep 8, 2026 — classified as 239 injuries, 298 malfunctions.
The most frequently reported specific device problem is “Fracture” (200 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported XIA 3 problems
Device problems
- Fracture200
- Break146
- Migration101
- Mechanical Problem71
- Detachment of Device or Device Component66
- Material Integrity Problem58
- Device Dislodged or Dislocated50
- Loose or Intermittent Connection48
Patient problems
- No Known Impact Or Consequence To Patient183
- Injury138
- No Clinical Signs, Symptoms or Conditions132
- Pain68
- No Consequences Or Impact To Patient55
- No Code Available52
- No Information22
- Insufficient Information17
XIA 3 models
93 models, most reported first. Each model has its own page with its reports, recalls and device details.
- XIA 3 48230000APPLIANCE, FIXATION, SPINAL INTERLAMINAL193 reports
- XIA 3 48232480Orthosis, spinal pedicle fixation, for degenerative disc disease33 reports
- XIA 3 48232601ORTHOSIS, SPINAL PEDICLE FIXATION16 reports
- XIA 3 482316540Orthosis, spinal pedicle fixation, for degenerative disc disease13 reports
- XIA 3 48231326ORTHOPEDIC MANUAL SURGICAL INSTRUMENT12 reports
- XIA 3 48233540ORTHOSIS, SPINAL PEDICLE FIXATION11 reports
- XIA 3 48232600Orthosis, spinal pedicle fixation, for degenerative disc disease10 reports
- XIA 3 48233600ORTHOSIS, SPINAL PEDICLE FIXATION10 reports
- XIA 3 482316545Orthosis, spinal pedicle fixation, for degenerative disc disease10 reports
- XIA 3 48233535Pedicle screw spinal system, adolescent idiopathic scoliosis10 reports
- XIA 3 48237028ORTHOPEDIC MANUAL SURGICAL INSTRUMENT10 reports
- XIA 3 482317545ORTHOSIS, SPINAL PEDICLE FIXATION9 reports
- XIA 3 482318570APPLIANCE, FIXATION, SPINAL INTERLAMINAL9 reports
- XIA 3 48236043ORTHOSIS, SPINAL PEDICLE FIXATION8 reports
- XIA 3 482318580APPLIANCE, FIXATION, SPINAL INTERLAMINAL8 reports
- XIA 3 48233480Orthosis, spondylolisthesis spinal fixation8 reports
- XIA 3 48237081ORTHOPEDIC MANUAL SURGICAL INSTRUMENT8 reports
- XIA 3 482318545Orthosis, spinal pedicle fixation, for degenerative disc disease7 reports
- XIA 3 482318590APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY7 reports
- XIA 3 48230141Orthosis, spinal pedicle fixation, for degenerative disc disease7 reports
- XIA 3 482317540ORTHOSIS, SPINAL PEDICLE FIXATION6 reports
- XIA 3 482317550Pedicle screw spinal system, adolescent idiopathic scoliosis6 reports
- XIA 3 482318550Orthosis, spondylolisthesis spinal fixation6 reports
- XIA 3 48235010APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY6 reports
- XIA 3 482317555Orthosis, spinal pedicle fixation, for degenerative disc disease5 reports
- XIA 3 482319580Orthosis, spinal pedicle fixation, for degenerative disc disease4 reports
- XIA 3 48233640ORTHOSIS, SPINAL PEDICLE FIXATION4 reports
- XIA 3 48230055ORTHOPEDIC MANUAL SURGICAL INSTRUMENT4 reports
- XIA 3 48237008ORTHOPEDIC MANUAL SURGICAL INSTRUMENT4 reports
- XIA 3 48231330ORTHOPEDIC MANUAL SURGICAL INSTRUMENT4 reports
- XIA 3 48236053APPLIANCE, FIXATION, SPINAL INTERLAMINAL3 reports
- XIA 3 482316535Orthosis, spinal pedicle fixation, for degenerative disc disease3 reports
- XIA 3 482317050Pedicle screw spinal system, adolescent idiopathic scoliosis3 reports
- XIA 3 482318540ORTHOSIS, SPINAL PEDICLE FIXATION3 reports
- XIA 3 48230133Orthosis, spinal pedicle fixation, for degenerative disc disease3 reports
- XIA 3 482365540ORTHOSIS, SPINAL PEDICLE FIXATION3 reports
- XIA 3 482306550APPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- XIA 3 482315530APPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- XIA 3 482315535APPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- XIA 3 482315540Orthosis, spinal pedicle fixation, for degenerative disc disease2 reports
- XIA 3 482316550Pedicle screw spinal system, adolescent idiopathic scoliosis2 reports
- XIA 3 482317580APPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- XIA 3 482317590ORTHOSIS, SPINAL PEDICLE FIXATION2 reports
- XIA 3 482319590ORTHOSIS, SPINAL PEDICLE FIXATION2 reports
- XIA 3 482365550APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY2 reports
- XIA 3 4823718570APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY2 reports
- XIA 3 482365535Orthosis, spinal pedicle fixation, for degenerative disc disease2 reports
- XIA 3 482335030Orthosis, spondylolisthesis spinal fixation2 reports
- XIA 3 48233550APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY2 reports
- XIA 3 48237056ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- XIA 3 48230233Orthosis, spondylolisthesis spinal fixation1 report
- XIA 3 48232110Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- XIA 3 48236030Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- XIA 3 48238070Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- XIA 3 48238090Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- XIA 3 482306540Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- XIA 3 482306555Pedicle screw spinal system, adolescent idiopathic scoliosis1 report
- XIA 3 482314540Orthosis, spondylolisthesis spinal fixation1 report
- XIA 3 482315030APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- XIA 3 482315040ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- XIA 3 482315550ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- XIA 3 482316560ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- XIA 3 482316570ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- XIA 3 482317535APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- XIA 3 482317570Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- XIA 3 482318500ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- XIA 3 482318560Orthosis, spondylolisthesis spinal fixation1 report
- XIA 3 482319540Orthosis, spondylolisthesis spinal fixation1 report
- XIA 3 482319550Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- XIA 3 482319570Orthosis, spondylolisthesis spinal fixation1 report
- XIA 3 482311550APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- XIA 3 482311590APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- XIA 3 48238110Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- XIA 3 48238100Pedicle screw spinal system, adolescent idiopathic scoliosis1 report
- XIA 3 482387570APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- XIA 3 482387580ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- XIA 3 4823717540APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- XIA 3 4823717555Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- XIA 3 4823717580ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- XIA 3 4823718590APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- XIA 3 48235480Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- XIA 3 482378560APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- XIA 3 482378580Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- XIA 3 482397012ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- XIA 3 482377590Orthosis, spondylolisthesis spinal fixation1 report
- XIA 3 482378570APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- XIA 3 482377580Orthosis, spondylolisthesis spinal fixation1 report
- XIA 3 IS2285XLPORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- XIA 3 IS2704XLPORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- XIA 3 48230190ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- XIA 3 48231311ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- XIA 3 48231320ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- XIA 3 48237011RORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
Recent XIA 3 adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 8, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50676257 ↗MalfunctionSep 8, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50676237 ↗InjurySep 8, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50676224 ↗MalfunctionAug 11, 2026Detachment of Device or Device Component
A company representative reported that the tulip of a Xia 3 Polyaxial Screw disengaged intra-operatively. The procedure was completed successfully with a 20 minute surgical delay.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50203473 ↗MalfunctionAug 11, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50203460 ↗InjuryJul 29, 2026Fracture
It was reported that a patient sustained a fall at home approximately 15 months post-operatively and experienced thoracic back pain. Imaging revealed that two Xia 3 Rods had fractured. The patient is scheduled to receive specialized medical care, however hospitalization nor surgical treatment have been required. This report captures the second of two Rods.
Patient problems: Back pain
MAUDE report 50074691 ↗InjuryJul 29, 2026Fracture
It was reported that a patient sustained a fall at home approximately 15 months post-operatively and experienced thoracic back pain. Imaging revealed that two Xia 3 Rods had fractured. The patient is scheduled to receive specialized medical care, however hospitalization nor surgical treatment have been required. This report captures the first of two Rods.
Patient problems: Back pain
MAUDE report 50074679 ↗InjuryJul 21, 2026Fracture
A HEALTH PROFESSIONAL REPORTED THAT A XIA 3 ROD WAS OBSERVED TO HAVE FRACTURED APPROXIMATELY 3 YEARS AND 8 MONTHS POST-OPERATIVELY. IT WAS FURTHER REPORTED THAT THE EVENT RESULTED IN HOSPITALIZATION OR ITS EXTENSION. REVISION SURGERY HAS NOT TAKEN PLACE NOR BEEN SCHEDULED AND THE PATIENT REPORTED NOT EXPERIENCING ANY PAIN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25898679 ↗InjuryJun 8, 2026Migration
A HEALTH PROFESSIONAL REPORTED THAT A PATIENT WAS REVISED APPROXIMATELY THREE WEEKS POST-OPERATIVELY TO ADDRESS A MIGRATED XIA 3 BLOCKER. THE PATIENT REPORTED EXPERIENCING A "CLICKING" SOUND DURING MOVEMENT AND X-RAY IMAGING REVEALED THE MIGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25437549 ↗InjuryApr 14, 2026Fracture
ADDITIONAL IMAGING PROVIDED FROM THE FIELD INDICATED THAT THREE RODS FRACTURED. THIS REPORT CAPTURES THE FIRST OF THREE RODS.
Patient problems: Back pain
MAUDE report 24877573 ↗MalfunctionApr 14, 2026Device Dislodged or Dislocated
A COMPANY REPRESENTATIVE REPORTED THAT THE TULIP OF A XIA 3 POLYAXIAL SCREW DISENGAGED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 24877426 ↗InjuryMar 25, 2026Insufficient Device Problem Information
A HEALTH PROFESSIONAL REPORTED THAT A PATIENT IMPLANTED WITH FOUR ES2 INTEGRATED BLADE SCREWS, FOUR XIA BLOCKERS, AND TWO MANTIS RODS EXPERIENCED AN INFECTION POST-OPERATIVELY. IT WAS FURTHER REPORTED THAT THE PATIENT WAS REVISED AND THE DEVICES WERE EXPLANTED. THIS REPORT CAPTURES THE FOURTH OF FOUR XIA BLOCKERS.
Patient problems: Unspecified Infection
MAUDE report 24691088 ↗InjuryMar 25, 2026Insufficient Device Problem Information
A HEALTH PROFESSIONAL REPORTED THAT A PATIENT IMPLANTED WITH FOUR ES2 INTEGRATED BLADE SCREWS, FOUR XIA BLOCKERS, AND TWO MANTIS RODS EXPERIENCED AN INFECTION POST-OPERATIVELY. IT WAS FURTHER REPORTED THAT THE PATIENT WAS REVISED AND THE DEVICES WERE EXPLANTED. THIS REPORT CAPTURES THE THIRD OF FOUR XIA BLOCKERS.
Patient problems: Unspecified Infection
MAUDE report 24691087 ↗InjuryMar 25, 2026Insufficient Device Problem Information
A HEALTH PROFESSIONAL REPORTED THAT A PATIENT IMPLANTED WITH FOUR ES2 INTEGRATED BLADE SCREWS, FOUR XIA BLOCKERS, AND TWO MANTIS RODS EXPERIENCED AN INFECTION POST-OPERATIVELY. IT WAS FURTHER REPORTED THAT THE PATIENT WAS REVISED AND THE DEVICES WERE EXPLANTED. THIS REPORT CAPTURES THE FIRST OF FOUR XIA BLOCKERS.
Patient problems: Unspecified Infection
MAUDE report 24691086 ↗InjuryMar 25, 2026Insufficient Device Problem Information
A HEALTH PROFESSIONAL REPORTED THAT A PATIENT IMPLANTED WITH FOUR ES2 INTEGRATED BLADE SCREWS, FOUR XIA BLOCKERS, AND TWO MANTIS RODS EXPERIENCED AN INFECTION POST-OPERATIVELY. IT WAS FURTHER REPORTED THAT THE PATIENT WAS REVISED AND THE DEVICES WERE EXPLANTED. THIS REPORT CAPTURES THE SECOND OF FOUR XIA BLOCKERS.
Patient problems: Unspecified Infection
MAUDE report 24691085 ↗
Other Stryker Corporation products
- RemB7 models · 3,073 reports
- Prime Series21 models · 1,548 reports · 2 recalls
- TARGET114 models · 1,077 reports
- ProCuity17 models · 368 reports · 13 recalls
- Spetzler-Malis20 models · 7 reports · 19 recalls
- SYNCHRO 28 models · 313 reports · 9 recalls
- Neptune E-SEP19 models · 412 reports · 7 recalls
- StrykeFlow4 models · 552 reports · 4 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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