Solidity Vertebral Body Replacement UU041-01-1621Recalls & reported problems
Ulrich Medical Usa, Inc. · Center piece, yellow, Ø 13mm, height 16-21.5mm, one fixed end cap, one variable end cap · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00814386022286), received between Dec 27, 2019 and Apr 9, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Collapse” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Collapse1
- Material Fragmentation1
Patient problems
- Failure of Implant2
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 9, 2021Material Fragmentation; Material Fragmentation
DURING INITIAL SURGERY, THE CAGE WAS IMPLANTED AND THE SURGEON WENT TO EXPAND IT, BUT TURNED THE INSERTER THE WRONG DIRECTION. THIS CAUSED THE LOCKING MECHANISM AND GEAR TEETH OF THE CAGE TO BREAK OFF. THE CAGE AND ALL PARTS WERE REMOVED AND REPLACED WITH A DIFFERENT CAGE.
Patient problems: Failure of Implant
MAUDE report 11640683 ↗MalfunctionDec 27, 2019Collapse; Collapse
6 WEEK POST-OP X-RAYS SHOW VBR HEIGHT REDUCTION.
Patient problems: Failure of Implant; No Known Impact Or Consequence To Patient
MAUDE report 9526660 ↗
Other Spinal Vertebral Body Replacement Device devices
- GIZA Corpectomy implant Giza, Diam 14 mm, 23-32 mm, 7-10 DegEden Spine Europe SA · Spinal Vertebral Body Replacement Device1 recall0 reports
- X-CORE 7160012Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- X-CORE 7220018Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- X-CORE 7160014Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- X-CORE 7180018Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- X-CORE 7180016Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- 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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