Skip to content

Invictus 15420-11Recalls & reported problems

Alphatec Spine, Inc. · Pivoting, OPEN-OPEN, Revision Connector, 11-14mm · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00190376283869), received between Oct 15, 2021 and Oct 15, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Unintended Movement” (1 report).

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Unintended Movement1

Patient problems

  • Insufficient Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 15, 2021Unintended Movement; Unintended Movement

    ON (B)(6) 2021, A PATIENT UNDERWENT A POSTERIOR LUMBAR SPINAL FUSION SURGERY. FOUR MONTHS POSTOPERATIVELY, IT WAS REPORTED A SCREW DISASSOCIATED FROM THE PIVOTING CONNECTOR. NO PATIENT INJURY REPORTED.

    Patient problems: Insufficient Information

    MAUDE report 12640712 ↗

Other APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices

All APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.