Precept 8801215Recalls & reported problems
Nuvasive, Inc. · PRECEPT Screwdriver, Polyaxial · Class 2
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 00887517350350), received between Oct 29, 2022 and Oct 29, 2022 — classified as 1 malfunction.
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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Fracture1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 29, 2022Fracture; Fracture
WHILE INSERTING A PEDICLE SCREW INTO L5, THE TIP OF THE SCREWDRIVER WAS BROKEN OFF IN THE SCREW HEAD. THE FRACTURED TIP COULD NOT BE RETRIEVED AND AS A RESULT THE TIP WAS RETAINED IN THE PATIENT. NO PATIENT HARM WAS REPORTED AS A RESULT OF THE REPORTED EVENT.
Patient problems: Foreign Body In Patient
MAUDE report 15695148 ↗
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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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