BASE 6955252Recalls & reported problems
Nuvasive, Inc. · BASE Ti Bolt, 5.0x25.0mm Variable · Class 2 · Implant
Data updated Oct 18, 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 00887517701831), received between May 22, 2017 and Nov 15, 2018 — classified as 2 malfunctions.
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
- Migration or Expulsion of Device1
Patient problems
- Failure of Implant1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 15, 2018Fracture; Fracture
ON (B)(6) 2016 PATIENT UNDERWENT A ANTERIOR LUMBAR INTERBODY FUSION PROCEDURE WITHOUT ANY REPORTED ISSUES. ON (B)(6) 2018 RADIOGRAPHS IDENTIFIED A FRACTURED INTER-FIXATION SCREW. NO PATIENT INJURY REPORTED NOR REVISION PROCEDURE PLANNED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8075627 ↗MalfunctionMay 22, 2017Migration or Expulsion of Device; Migration or Expulsion of Device
ON (B)(6) 2017 A (B)(6) Y/O FEMALE UNDERWENT A VERTEBRAL BODY REPLACEMENT. ON (B)(6) 2017 FOLLOW UP RADIOGRAPHS SHOWED THE INTERFIXATED SCREW BACKING OUT AND CAGE MIGRATION AT L4-L5. AS PER INITIAL REPORTER NO REVISION PROCEDURE IS PLANNED AT THIS TIME.
Patient problems: Failure of Implant
MAUDE report 6583711 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page