InvictusRecalls & reported problems across all models
Alphatec Spine, Inc. · 96 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 448
- Deaths reported
- 0
- Injuries reported
- 123
- Recalls
- 0
We found 96 models of Invictus by Alphatec Spine, Inc. in the FDA's device registry (GUDID). Together they are named in 448 adverse event reports in the FDA's MAUDE database, received between Jan 29, 2019 and Sep 29, 2026 — classified as 123 injuries, 325 malfunctions.
The most frequently reported specific device problem is “Break” (313 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 Invictus problems
Device problems
- Break313
- Material Separation155
- Device Dislodged or Dislocated47
- Fracture41
- Detachment of Device or Device Component23
- Separation Failure5
- Unintended Movement5
- Device Slipped4
Patient problems
- No Clinical Signs, Symptoms or Conditions288
- Failure of Implant75
- Insufficient Information39
- Foreign Body In Patient31
- No Known Impact Or Consequence To Patient12
- Device Embedded In Tissue or Plaque5
- Pain4
- Bone Fracture(s)2
Invictus models
96 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Invictus 15100Thoracolumbosacral pedicle screw system65 reports
- Invictus 17950-225SCREWDRIVER54 reports
- Invictus 17140Orthopedic stereotaxic instrument44 reports
- Invictus 17950-NOrthopedic stereotaxic instrument34 reports
- Invictus 17109-055TAP, BONE22 reports
- Invictus 17026SCREWDRIVER21 reports
- Invictus 17111SCREWDRIVER20 reports
- Invictus 17110SCREWDRIVER16 reports
- Invictus 17806SCREWDRIVER13 reports
- Invictus 17138SCREWDRIVER9 reports
- Invictus 17830SCREWDRIVER9 reports
- Invictus 19807-30TAP, BONE8 reports
- Invictus 17109-045TAP, BONE6 reports
- Invictus 17139-045-NOrthopedic stereotaxic instrument5 reports
- Invictus 17139-055-NOrthopedic stereotaxic instrument5 reports
- Invictus 55405-090-080APPLIANCE, FIXATION, SPINAL INTERLAMINAL5 reports
- Invictus 17001-01PROBE4 reports
- Invictus 15025-075-045APPLIANCE, FIXATION, SPINAL INTERLAMINAL3 reports
- Invictus 15025-075-050APPLIANCE, FIXATION, SPINAL INTERLAMINAL3 reports
- Invictus 16021ORTHOPEDIC MANUAL SURGICAL INSTRUMENT3 reports
- Invictus 19000-55-30Posterior cervical screw system3 reports
- Invictus 55005-105-090APPLIANCE, FIXATION, SPINAL INTERLAMINAL3 reports
- Invictus 55405-090-090APPLIANCE, FIXATION, SPINAL INTERLAMINAL3 reports
- Invictus 55405-090-100APPLIANCE, FIXATION, SPINAL INTERLAMINAL3 reports
- Invictus 55405-095-100Thoracolumbosacral pedicle screw system3 reports
- Invictus 17850-225SCREWDRIVER3 reports
- Invictus 15004-095-090APPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- Invictus 17010SCREWDRIVER2 reports
- Invictus 17100-18-2ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- Invictus 15600Thoracolumbosacral pedicle screw system2 reports
- Invictus 15620APPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- Invictus 15610APPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- Invictus 19000-35-24Posterior cervical screw system2 reports
- Invictus 19000-55-26Posterior cervical screw system2 reports
- Invictus 55005-095-080APPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- Invictus 17908SCREWDRIVER2 reports
- Invictus 55405-105-090Thoracolumbosacral pedicle screw system2 reports
- Invictus 15025-055-035Thoracolumbosacral pedicle screw system1 report
- Invictus 15025-055-045Thoracolumbosacral pedicle screw system1 report
- Invictus 15025-065-045APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 15025-065-050APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 15025-095-050Thoracolumbosacral pedicle screw system1 report
- Invictus 15004-055-035Thoracolumbosacral pedicle screw system1 report
- Invictus 15004-065-045Thoracolumbosacral pedicle screw system1 report
- Invictus 15004-085-080APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 15004-085-090Thoracolumbosacral pedicle screw system1 report
- Invictus 15004-095-080APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 15004-105-090APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 15004-105-100Thoracolumbosacral pedicle screw system1 report
- Invictus 15074-095-090Thoracolumbosacral pedicle screw system1 report
- Invictus 16015-04SCREWDRIVER1 report
- Invictus 15200-55-500APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 15406-30Thoracolumbosacral pedicle screw system1 report
- Invictus 15005-075-040Thoracolumbosacral pedicle screw system1 report
- Invictus 15005-075-050APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 17109-065TAP, BONE1 report
- Invictus 17109-075TAP, BONE1 report
- Invictus 17003PROBE1 report
- Invictus 17137ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Invictus 17100-18-1ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Invictus 17100-25-2ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Invictus 15054-065-040APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 15704-065-040APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 15704-065-045Thoracolumbosacral pedicle screw system1 report
- Invictus 15250-60-400APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 17139-055Orthopedic stereotaxic instrument1 report
- Invictus 15705-075-045APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 15705-085-050APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 18100Posterior cervical screw system1 report
- Invictus 15001-085-040APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 15001-085-090Thoracolumbosacral pedicle screw system1 report
- Invictus 17182ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Invictus 17125ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- Invictus 15295-55-080APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 15295-55-120Thoracolumbosacral pedicle screw system1 report
- Invictus 17402APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 17412Thoracolumbosacral pedicle screw system1 report
- Invictus 15420-11APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 19807-35TAP, BONE1 report
- Invictus 19000-35-20Posterior cervical screw system1 report
- Invictus 19000-40-18Posterior cervical screw system1 report
- Invictus 19000-55-40Posterior cervical screw system1 report
- Invictus 19003-35-30Posterior cervical screw system1 report
- Invictus 19003-35-32Posterior cervical screw system1 report
- Invictus 19807-35-NOrthopedic stereotaxic instrument1 report
- Invictus 17139-065-NOrthopedic stereotaxic instrument1 report
- Invictus 19500-48Posterior cervical screw system1 report
- Invictus 19500-56Posterior cervical screw system1 report
- Invictus 17092-01-01Orthopedic manual surgical instrument1 report
- Invictus 55005-085-100APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 55005-105-080APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 55203-075-045Thoracolumbosacral pedicle screw system1 report
- Invictus 55203-065-045Thoracolumbosacral pedicle screw system1 report
- Invictus 55475-105-090APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 55475-105-100APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- Invictus 17109-045-GTAP, BONE1 report
Recent Invictus adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 29, 2026Break
A patient underwent revision surgery for Proximal Junction Kyphosis. Intraoperatively, a previously implanted screw was found to be fractured and was removed.
Patient problems: Spinal deformity
MAUDE report 50936647 ↗InjurySep 29, 2026Fracture
Patient problems: Spinal deformity
MAUDE report 50936608 ↗MalfunctionSep 24, 2026Break; Material Separation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50892126 ↗MalfunctionSep 24, 2026Break; Material Separation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50891994 ↗MalfunctionSep 24, 2026Break; Material Separation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50891272 ↗MalfunctionSep 24, 2026Break; Material Separation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50890246 ↗MalfunctionSep 24, 2026Break; Material Separation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50886589 ↗MalfunctionSep 24, 2026Break; Material Separation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50886419 ↗MalfunctionSep 24, 2026Break; Material Separation
It was reported that the tip broke off during final tightening. The tip was retrieved.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50885672 ↗InjurySep 23, 2026Separation Failure; Difficult or Delayed Separation
While attempting to deploy the tulip onto the screw shank, the gold button reportedly did not release the tulip. During an attempt to seat the tulip head onto the screw shank, the L5 pedicle fractured. The patient is asymptomatic.
Patient problems: Vertebral Fracture
MAUDE report 50869884 ↗MalfunctionSep 16, 2026Break; Material Separation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50790714 ↗MalfunctionSep 14, 2026Break; Material Separation
It was reported that the tip of the driver broke off during a case. The tip was retrieved.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50759572 ↗MalfunctionSep 14, 2026Break; Material Separation
It was reported that the tip of the driver broke off during a case. The tip was retrieved.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50758627 ↗MalfunctionSep 14, 2026Break; Material Separation
It was reported that the tip of the driver sheared off during a case. The tip was retrieved.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50754842 ↗MalfunctionSep 10, 2026Break; Material Separation
It was reported that the tip of the driver is broken.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50718143 ↗
Other Alphatec Spine, Inc. products
- IdentiTi31 models · 68 reports · 1 recall
- ATEC Lateral Navigation Disc Prep Instruments2 models · 0 reports · 2 recalls
- Calibrate44 models · 40 reports · 1 recall
- Arsenal18 models · 86 reports
- Illico20 models · 69 reports
- AMP5 models · 4 reports · 1 recall
- Insignia34 models · 54 reports
- Trestle Luxe24 models · 38 reports
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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