Invictus 55005-105-090Recalls & reported problems
Alphatec Spine, Inc. · Cannulated Iliac Favored Angle Screw, 10.5mm X 90mm · Class 2 · Implant
All models of Invictus (96)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00190376404752), received between Jan 30, 2025 and Jun 17, 2025 — classified as 3 injuries.
The most frequently reported specific device problem is “Break” (3 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, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break3
Patient problems
- Failure of Implant3
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJun 17, 2025Break; Break
IT WAS REPORTED THAT THREE ILIAC SCREWS BROKE AT THE NECK POSTOPERATIVELY. THE INITIAL SURGERY OCCURRED ON (B)(6) 2024. POSTOPERATIVELY, TWO OF THE SCREWS BROKE AT THE NECK, AND REVISION SURGERY OCCURRED ON (B)(6) 2025 TO REMOVE THE BROKEN SCREWS. DURING THIS SURGERY, FOUR POINTS OF ILIAC FIXATION WERE ADDED. THE THIRD SCREW BROKE AT THE NECK POSTOPERATIVELY AND WAS REMOVED ON (B)(6) 2025 AND REPLACED WITH THE SAME SIZE. THIS IS REPORT 2 OF 3.
Patient problems: Failure of Implant
MAUDE report 22235012 ↗InjuryJun 17, 2025Break; Break
A PATIENT UNDERWENT SPINAL SURGERY ON (B)(6) 2024. DURING A POSTOPERATIVE VISIT, IMAGING SHOWED THAT TWO CANNULATED ILIAC SCREWS HAD BROKEN AT THE NECK. A REVISION SURGERY WAS PERFORMED TO REMOVE AND REPLACE THEM. FOUR MONTHS LATER, A POLYAXIAL ILIAC SCREW WAS ALSO FOUND TO BE BROKEN AT THE NECK. A SECOND REVISION SURGERY WAS PERFORMED TO REMOVE AND REPLACE THE SCREW. THIS IS REPORT 1 OF 3.
Patient problems: Failure of Implant
MAUDE report 22235004 ↗InjuryJan 30, 2025Break; Break
IT WAS REPORTED THAT A SCREW BROKE AND NEEDED TO BE REMOVED FROM THE PATIENT.
Patient problems: Failure of Implant; Insufficient Information
MAUDE report 21274184 ↗
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- XIA 3 48230000Stryker Corporation · APPLIANCE, FIXATION, SPINAL INTERLAMINAL193 reports
- VIPER 186715000Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 death167 reports
- NA 04.614.014Synthes GmbH · APPLIANCE, FIXATION, SPINAL INTERLAMINAL80 reports
- EXPEDIUM VIPER 196789480Depuy Spine, LLC · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
- NA 04.615.014Synthes GmbH · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
- Arsenal Deformity Spinal Fixation System 47127Alphatec Spine, Inc. · APPLIANCE, FIXATION, SPINAL INTERLAMINAL66 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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