SP-FIX 588.026Recalls & reported problems
Globus Medical, Inc. · SP-Fix Double tab Locking Plate, 26mm · Class 2
- 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 00849044092257), received between Nov 20, 2025 and Nov 20, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Migration” (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.
Reports received per month
Most reported problems
Device problems
- Migration1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 20, 2025Migration; Migration
IT WAS REPORTED THAT A PATIENT HAD MULTIPLE LEVELS OF SP FIX PLATES AND BARRELS PLACED. THE TOP LEVEL WHICH WAS A DOUBLE TAB LOCKING PLATE WHICH BECAME SEPARATED FROM THE BARREL.
Patient problems: Failure of Implant
MAUDE report 23608426 ↗
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- ZIP LPAurora Spine, Inc. · Spinous Process Plate1 report
- Axle Interspinous Fusion System X060-0241Xtant Medical Holdings, Inc. · Spinous process plate1 report
- UniVise 48590035Stryker Corporation · Spinous process plate1 report
- ZIP ULTRAAurora Spine, Inc. · Spinous Process Plate1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.