NA 698273327Recalls & reported problems
Depuy Spine, LLC · MODIFIED INSTRUMENT STANDARD RASP 7mm · Class 1
Data updated Oct 16, 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 10705034448350), received between Oct 10, 2019 and Oct 10, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- 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.
MalfunctionOct 10, 2019Break; Break
LIBERTAS: BROKEN INSTRUMENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9174428 ↗
Other RASP, SURGICAL, GENERAL & PLASTIC SURGERY devices
- Progressive proximal rasp PIP 211-A43000Keri Medical SA · Rasp, Surgical, General & Plastic Surgery4 reports
- VG2 273340107Medos International Sàrl · RASP, SURGICAL, GENERAL & PLASTIC SURGERY2 reports
- VG2 273340106Medos International Sàrl · RASP, SURGICAL, GENERAL & PLASTIC SURGERY2 reports
- VG2 273340108Medos International Sàrl · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- CONCORDE 287903001Depuy Spine, LLC · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- CONCORDE 287903003Depuy Spine, LLC · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- Innomed, Inc. 3004-01Innomed, Inc. · Rasp, Surgical, General & Plastic Surgery1 report
- VG2 273340109Medos International Sàrl · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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