obeliscPRO™ vertebral body replacement CS 2915-10Recalls & reported problems
Ulrich GmbH & Co. KG · obelisc lateral end piece, green, length 45 mm, angle 10° · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 04052536113767), received between Jun 2, 2021 and Jun 2, 2021 — classified as 2 injuries, 2 malfunctions.
The most frequently reported specific device problem is “Connection Problem” (4 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.
Most reported problems
Device problems
- Connection Problem4
Patient problems
- Failure of Implant4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 2, 2021Connection Problem; Connection Problem
OBELISC ATTACHMENT PLATE DETACHED POST-OPERATIVELY. REPORT 2 OF 3.
Patient problems: Failure of Implant
MAUDE report 11924599 ↗InjuryJun 2, 2021Connection Problem; Connection Problem
OBELISC ATTACHMENT PLATE DETACHED POST-OPERATIVELY. REPORT 2 OF 3.
Patient problems: Failure of Implant
MAUDE report 11924590 ↗InjuryJun 2, 2021Connection Problem; Connection Problem
OBELISC ATTACHMENT PLATE DETACHED POST-OPERATIVELY. REPORT 3 OF 3.
Patient problems: Failure of Implant
MAUDE report 11924582 ↗MalfunctionJun 2, 2021Connection Problem; Connection Problem
OBELISC ATTACHMENT PLATE DETACHED POST-OPERATIVELY. REPORT 3 OF 3.
Patient problems: Failure of Implant
MAUDE report 11924580 ↗
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- GIZA Corpectomy implant Giza, Diam 14 mm, 18-22 mm, 2-5 DegEden Spine Europe SA · Spinal Vertebral Body Replacement Device1 recall0 reports
- GIZA Corpectomy implant Giza, Diam 14 mm, 23-32 mm, 2-5 DegEden Spine Europe SA · Spinal Vertebral Body Replacement Device1 recall0 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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