Solidity Vertebral Body Replacement UU041-01-1927Recalls & reported problems
Ulrich Medical Usa, Inc. · Center piece, turquoise, Ø 13mm, height 19-27.5mm, 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
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00814386022293), received between Dec 27, 2019 and Oct 27, 2025 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Collapse” (2 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.
Reports received per month
Most reported problems
Device problems
- Collapse2
- Loosening of Implant Not Related to Bone-Ingrowth1
Patient problems
- Failure of Implant2
- Insufficient Information1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryOct 27, 2025Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth
DURING A POST OPERATIVE FOLLOW UP, THE VBR CAGE PREVIOUSLY IMPLANTED HAD BECOME LOOSE AFTER A SURGICAL WASHOUT WAS CONDUCTED. THE CAGE WAS REMOVED AND REPLACED WITH A LARGER ONE. COLLAPSE OR SUBSIDENCE WAS NOT REPORTED. THERE WAS NO EFFECT ON THE PATIENT OTHER THAN THE UNEXPECTED DELAY.
Patient problems: Insufficient Information
MAUDE report 23393375 ↗MalfunctionJan 10, 2020Collapse; Collapse
6 WEEK POST-OP X-RAYS SHOWED VBR HEIGHT REDUCTION. NO REVISION SURGERY HAS OCCURRED OR BEEN SCHEDULED AS OF THIS DATE. THE PATIENT'S CONDITION IS BEING MONITORED.
Patient problems: Failure of Implant
MAUDE report 9577962 ↗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 9526656 ↗
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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