Invictus 19000-55-26Recalls & reported problems
Alphatec Spine, Inc. · POLYAXIAL SCREW, 5.5mm X 26mm · Class 2 · Implant
All models of Invictus (96)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00190376303673), received between Jul 7, 2025 and Jul 7, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Fracture” (2 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture2
Patient problems
- Failure of Implant2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJul 7, 2025Fracture; Fracture
A PATIENT UNDERWENT A POSTERIOR CERVICAL FUSION PROCEDURE AT LEVEL C1-C7. DURING A POSTOPERATIVE VISIT, RADIOGRAPH IMAGING REVEALED BILATERAL SCREW FRACTURES AT THE C7 LEVEL, WITH BREAKAGE OCCURRING AT THE SCREW NECKS. THE PATIENT REMAINS ASYMPTOMATIC. REVISION SURGERY IS PLANNED TO REMOVE THE FRACTURED SCREWS AND EXTEND THE SPINAL CONSTRUCT TO T3. THIS IS REPORT 2 OF 2.
Patient problems: Failure of Implant
MAUDE report 22421561 ↗InjuryJul 7, 2025Fracture; Fracture
A PATIENT UNDERWENT A POSTERIOR CERVICAL FUSION PROCEDURE AT LEVEL C1-C7. DURING A POSTOPERATIVE VISIT, RADIOGRAPH IMAGING REVEALED BILATERAL SCREW FRACTURES AT THE C7 LEVEL, WITH BREAKAGE OCCURRING AT THE SCREW NECKS. THE PATIENT REMAINS ASYMPTOMATIC. REVISION SURGERY IS PLANNED TO REMOVE THE FRACTURED SCREWS AND EXTEND THE SPINAL CONSTRUCT TO T3.
Patient problems: Failure of Implant
MAUDE report 22421460 ↗
Other Posterior cervical screw system devices
- INFINITY™ Occipitocervical Upper Thoracic System 3604026Medtronic Sofamor Danek, Inc. · Orthosis, cervical pedicle screw spinal fixation2 recalls1 report
- CONNECTOR 79-2002Orthofix US LLC · Posterior cervical screw system1 recall0 reports
- INFINITY™ Occipitocervical Upper Thoracic System 3604532Medtronic Sofamor Danek, Inc. · Orthosis, cervical pedicle screw spinal fixation1 recall0 reports
- INFINITY™ Occipitocervical Upper Thoracic System 3604024Medtronic Sofamor Danek, Inc. · Orthosis, cervical pedicle screw spinal fixation1 recall0 reports
- CONNECTOR 79-2003Orthofix US LLC · Posterior cervical screw system1 recall0 reports
- INFINITY™ Occipitocervical Upper Thoracic System 360PT4022Medtronic Sofamor Danek, Inc. · Orthosis, cervical pedicle screw spinal fixation1 recall0 reports
- OASYS 48551000Stryker Corporation · Orthosis, cervical pedicle screw spinal fixation45 reports
- SYMPHONY 1020-35-112Medos International Sàrl · Posterior cervical screw system6 deaths15 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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