CAPRI™ Corpectomy Cage System 7512-21624L0-G3Recalls & reported problems
VB Spine LLC · Corpectomy Cage with Set Screw, Size 13x16mm, 20-24mm, 0°, 0-20° · Class 2 · Implant
All models of CAPRI Corpectomy Cage System (20)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888857371101), received between Jan 11, 2021 and Jan 11, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (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
- Fracture1
- Migration1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 11, 2021Fracture; Migration; Fracture; Migration
IT WAS REPORTED THAT THE PATIENT EXPERIENCED PAIN POST OPERATIVELY AND AN X-RAY INDICATED THE CAGE FRACTURED. THE PATIENT WAS REVISED.
Patient problems: Pain
MAUDE report 11149924 ↗
Other Spinal vertebral body replacement device - Cervical devices
- CAPRI™ Corpectomy Cage System 7512-21846L0-G3VB Spine LLC · Spinal vertebral body replacement device - Cervical1 report
- X-CORE 7160022P2Nuvasive, Inc. · Spinal vertebral body replacement device - Cervical1 report
- Ascend 156-12-200Alphatec Spine, Inc. · Spinal vertebral body replacement device - Cervical1 report
- CAPRI™ Corpectomy Cage System 7512-21636L0-G3VB Spine LLC · Spinal vertebral body replacement device - Cervical1 report
- CAPRI™ Corpectomy Cage System 7512-21421L0-G3VB Spine LLC · Spinal vertebral body replacement device - Cervical1 report
- Ascend 155-0-12-35Alphatec Spine, Inc. · Spinal vertebral body replacement device - Cervical1 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 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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