XPAND 116.109Recalls & reported problems
Globus Medical, Inc. · XPand Corpectomy Spacer Small 12x14 3.5/3.5°, 26-30mmE · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00849044022537), received between Dec 31, 2025 and Dec 31, 2025 — classified as 1 malfunction.
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
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 31, 2025Migration; Migration
IT WAS REPORTED THAT ON (B)(6) 2025, THE ORIGINAL SURGERY WAS PERFORMED. THE PRE-OPERATIVE MEASUREMENT SHOWED A HEIGHT OF APPROXIMATELY 27 MM, SO A 26 MM XPAND WAS SELECTED. THE POST-IMPLANTATION X-RAY CONFIRMED THAT BOTH THE DEPTH AND HEIGHT WERE APPROPRIATE, AND THE SPIKES WERE WELL SEATED AGAINST THE SUPERIOR AND INFERIOR ENDPLATES. HOWEVER, ABOUT ONE MONTH LATER, SUBSIDENCE WAS OBSERVED, SO THE IMPLANT WAS REMOVED AND REPLACED WITH ANOTHER BRAND OF CAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23936036 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.