VuePoint 7905428Recalls & reported problems
Nuvasive, Inc. · VuePoint Screw, 4x28mm Multi Axial · Class 2 · Implant
All models of VuePoint (26)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00887517180056), received between Aug 18, 2021 and Jul 18, 2024 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Separation 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.
Reports received per month
Most reported problems
Device problems
- Separation Problem4
- Detachment of Device or Device Component2
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Fall2
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 18, 2024Detachment of Device or Device Component; Separation Problem; Detachment of Device or Device Component; Separation Problem
IT WAS REPORTED THAT ON AN UNKNOWN DATE A PATIENT SUSTAINED A FALL. THE PATIENT RETURNED TO THE CLINIC FOR EVALUATION WHERE RADIOGRAPHS IDENTIFIED TWO PEDICLE SCREW TULIPS HAD SEPARATED FROM THE SCREW SHANKS. ADDITIONAL INFORMATION A REVISION PROCEDURE TOOK PLACE ON (B)(6) 2024 WHERE HARDWARE WAS REMOVED. NO OTHER INFORMATION PROVIDED.
Patient problems: Fall; No Clinical Signs, Symptoms or Conditions
MAUDE report 19774341 ↗MalfunctionJul 18, 2024Detachment of Device or Device Component; Separation Problem; Detachment of Device or Device Component; Separation Problem
IT WAS REPORTED THAT ON AN UNKNOWN DATE A PATIENT SUSTAINED A FALL. THE PATIENT RETURNED TO THE CLINIC FOR EVALUATION WHERE RADIOGRAPHS IDENTIFIED TWO PEDICLE SCREW TULIPS HAD SEPARATED FROM THE SCREW SHANKS. ADDITIONAL INFORMATION A REVISION PROCEDURE TOOK PLACE ON (B)(6) 2024 WHERE HARDWARE WAS REMOVED. NO OTHER INFORMATION PROVIDED. (NEW OR UPDATED INFORMATION LISTED ON SECTION H10).
Patient problems: Fall; No Clinical Signs, Symptoms or Conditions
MAUDE report 19774335 ↗MalfunctionAug 18, 2021Separation Problem; Separation Problem
NEW INFORMATION IDENTIFIED ON H10.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12338037 ↗MalfunctionAug 18, 2021Separation Problem; Separation Problem
NEW INFORMATION IDENTIFIED ON H10.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12338024 ↗
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- EXPEDIUM VIPER 196789480Depuy Spine, LLC · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
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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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