VuePoint 7905836Recalls & reported problems
Nuvasive, Inc. · VP Screw, 3.5.x36mm Fav Ang Part Thread · Class 2 · Implant
Data updated Oct 13, 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 00887517182791), received between Oct 19, 2023 and Oct 19, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 19, 2023Fracture; Fracture
ON (B)(6) 2018 A PATIENT UNDERWENT A CERVICAL SPINAL FUSION PROCEDURE ON UNCONFIRMED LEVELS OF THE SPINE. THE SURGERY WAS COMPLETED WITHOUT ISSUE. ON (B)(6) 2023 THE PATIENT UNDERWENT A REVISION PROCEDURE TO ADDRESS THREE FRACTURED. DURING THE REVISION PORTIONS OF THE FRACTURED SCREWS WERE REMOVED BUT NOT ALL FRACTURED PORTIONS COULD BE RETRIEVED FROM THE VERTEBRAL BODIES AND WERE SUBSEQUENTLY LEFT IN SITU. THE REVISION WAS COMPLETED WITH NO ADDITIONAL REPORTED ISSUES TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17970670 ↗MalfunctionOct 19, 2023Fracture; Fracture
ON (B)(6) 2018, A PATIENT UNDERWENT A SPINAL FUSION PROCEDURE ON UNCONFIRMED LEVELS OF THE SPINE. THE SURGERY WAS COMPLETED WITHOUT ISSUE. ON (B)(6) 2023, THE PATIENT UNDERWENT A REVISION PROCEDURE TO ADDRESS THREE FRACTURED. DURING THE REVISION PORTIONS OF THE FRACTURED SCREWS WERE REMOVED BUT NOT ALL FRACTURED PORTIONS COULD BE RETRIEVED FROM THE VERTEBRAL BODIES AND WERE SUBSEQUENTLY LEFT IN SITU. THE REVISION WAS COMPLETED WITH NO ADDITIONAL REPORTED ISSUES TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17970564 ↗
Other APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices
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- EXPEDIUM VERSE 199721001Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL227 reports
- XIA 3 48230000Stryker Corporation · APPLIANCE, FIXATION, SPINAL INTERLAMINAL193 reports
- VIPER 186715000Medos International Sàrl · APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 death167 reports
- NA 04.614.014Synthes GmbH · APPLIANCE, FIXATION, SPINAL INTERLAMINAL80 reports
- EXPEDIUM VIPER 196789480Depuy Spine, LLC · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
- NA 04.615.014Synthes GmbH · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
- Arsenal Deformity Spinal Fixation System 47127Alphatec Spine, Inc. · APPLIANCE, FIXATION, SPINAL INTERLAMINAL66 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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