BASE 6951815Recalls & reported problems
Nuvasive, Inc. · BASE Ti Implant, 8x34x24mm 15° · Class 2 · Implant
Data updated Oct 18, 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 00887517700827), received between Aug 18, 2020 and Aug 18, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Migration” (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
- Migration1
Patient problems
- Bone Fracture(s)1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 18, 2020Migration; Migration
ON (B)(6) 2020 PATIENT UNDERWENT A ANTERIOR LUMBAR INTERBODY FUSION PROCEDURE AT L5-S1 LEVELS. ON (B)(6) 2020, WHILE AT THE HOSPITAL THE PATIENT WAS WALKING AND FELT A "POP". X-RAYS REVELED A SCREW BACK OUT AND PARS SEPARATION. ON (B)(6) 2020, THE SECOND PART OF THE PROCEDURE WAS PERFORMED, WHERE THE CONSTRUCT WAS BACKED UP WITH PERCUTANEOUS PEDICLE SCREWS. PATIENT WILL CONTINUE TO BE MONITORED, FOR ANY FURTHER L5 SCREW MOVEMENT. REPORTEDLY, THE PATIENT IS DOING WELL AFTER POSTERIOR STABILIZATION.
Patient problems: Bone Fracture(s); Pain
MAUDE report 10422792 ↗
Other Intervertebral fusion device with integrated fixation, lumbar devices
- PIVOX™ Oblique Lateral Spinal System 2161001Medtronic Sofamor Danek, Inc. · Intervertebral fusion device with integrated fixation, lumbar182 reports
- IdentiTi 232-10-85-300Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall8 reports
- IdentiTi 232-10-85-250Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall5 reports
- IdentiTi 132-10-85-300Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall3 reports
- MectaLIF Anterior 03.30.301Medacta International SA · Intervertebral Fusion Device With Integrated Fixation, Lumbar1 recall2 reports
- IdentiTi 232-10-85-350Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall2 reports
- IdentiTi 232-11-90-350Alphatec Spine, Inc. · Intervertebral fusion device with integrated fixation, lumbar1 recall1 report
- MectaLIF Anterior 03.30.302Medacta International SA · Intervertebral Fusion Device With Integrated Fixation, Lumbar1 recall1 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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