CANOPY 1102.4011Recalls & reported problems
Globus Medical, Inc. · CANOPY Shelf Plate, Adjacent, 11mm · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 00889095027730), received between Mar 5, 2024 and Mar 5, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Product Quality Problem” (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
- Product Quality Problem1
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.
MalfunctionMar 5, 2024Product Quality Problem; Product Quality Problem
IT WAS REPORTED THAT A REVISION SURGERY WAS NEEDED DUE TO THE PATIENT FRACTURE AT C6, AND A CANOPY SHELF PLATE WAS FOUND BROKEN. THIS EVENT OCCURRED IN JAPAN.
Patient problems: Insufficient Information
MAUDE report 18837796 ↗
Other ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL devices
- Centerpiece Plate Fixation System 8532065Medtronic Sofamor Danek, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL13 reports
- Centerpiece Plate Fixation System 8532067Medtronic Sofamor Danek, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL11 reports
- Xspan Laminoplasty Fixation System X085-0250-STRXtant Medical Holdings, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL6 reports
- Centerpiece Plate Fixation System G8532067Medtronic Sofamor Danek, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL3 reports
- Xspan Laminoplasty Fixation System X085-0150-STRXtant Medical Holdings, Inc. · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL3 reports
- ESCALATE 48570300Stryker Corporation · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL2 reports
- Gallery™ Laminoplasty System 14-523101Biomet Spine LLC · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL1 report
- Gallery™ Laminoplasty System 14-523100Biomet Spine LLC · ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL1 report
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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