VuePoint 7906340Recalls & reported problems
Nuvasive, Inc. · VuePoint OCT Plate, 40mm Keel · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517184856), received between Apr 11, 2017 and Apr 11, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment Of Device Component” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Detachment Of Device Component1
Patient problems
- Failure of Implant1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 11, 2017Detachment Of Device Component; Detachment Of Device Component
ON (B)(6) 2011 A (B)(6) YEAR-OLD FEMALE PATIENT WITH SIGNIFICANT PRIOR SURGICAL HISTORY RECEIVED SEGMENTAL POSTERIOR FIXATION FROM OCCIPUT - C2 AS WELL AS C3-T3. 6-8 WEEKS AFTER INDEX SURGERY, THE FIXATION ROD SEPARATED FROM THE OCCIPITAL PLATE. THE DETACHMENT OF THE ROD FROM THE OCCIPUT WAS NOT REPAIRED.
Patient problems: Failure of Implant; No Consequences Or Impact To Patient
MAUDE report 6481794 ↗
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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 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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