Armada 7459014Recalls & reported problems
Nuvasive, Inc. · Armada Ti Screwdriver · Class 2
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 00887517484505), received between Aug 11, 2022 and Aug 11, 2022 — 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.
Most reported problems
Device problems
- Fracture2
Patient problems
- Foreign Body In Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 11, 2022Fracture; Fracture
DURING A SPINAL PROCEDURE ON AN UNKNOWN DATE, THE TIP FRACTURED OFF WHILE DRIVING THE SCREW AND WAS LEFT IN-SITU. NO PATIENT HARM WAS REPORTED AS A RESULT OF THE REPORTED EVENT.
Patient problems: Foreign Body In Patient
MAUDE report 15211093 ↗MalfunctionAug 11, 2022Fracture; Fracture
DURING A SPINAL PROCEDURE ON AN UNKNOWN DATE, THE TIP FRACTURED OFF WHILE DRIVING THE SCREW AND WAS LEFT IN-SITU. NO PATIENT HARM WAS REPORTED AS A RESULT OF THE REPORTED EVENT.
Patient problems: Foreign Body In Patient
MAUDE report 15211061 ↗
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- NIM Trivantage® 8229707Medtronic Xomed, Inc. · STIMULATOR, NERVE1 recall142 reports
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- NIM TriVantage® 8229706Medtronic Xomed, Inc. · STIMULATOR, NERVE2 recalls78 reports
- NIM-Response® 8253002Medtronic Xomed, Inc. · STIMULATOR, NERVE171 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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