NA 698340577Recalls & reported problems
Depuy Spine, LLC · MODIFIED INSTRUMENT PROBE · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10705034466262), received between Dec 28, 2022 and Mar 6, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (3 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
- Break3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 6, 2023Break; Break
IT WAS REPORTED THAT ON (B)(6) 2023, DURING THE USE OF THE BALL TIP THE FEELER BROKE. NO SURGICAL DELAY. PROCEDURE OUTCOME WAS UNKNOWN. NO PATIENT CONSEQUENCES. THIS REPORT IS FOR ONE (1) MODIFIED INSTRUMENT PROBE. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16485042 ↗MalfunctionJan 24, 2023Break; Break
IT WAS REPORTED THAT ON (B)(6) 2023, A FEELING PROBE BROKE DURING SURGERY. THE PROBE WAS RETRIEVED. THERE WAS NO SURGICAL DELAY AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO CLINICAL OUTCOME. THIS COMPLAINT INVOLVES ONE (1) DEVICE. THIS REPORT IS FOR ONE (1) MODIFIED PROBE. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16236814 ↗MalfunctionDec 28, 2022Break; Break
IT WAS REPORTED THAT ON UNKNOWN DATE, FEELING PROBE BROKE DURING INSPECTION OF A PEDICLE. NO PATIENT CONSEQUENCES WAS THERE. THIS COMPLAIN INVOLVES ONE(1) DEVICE. THIS REPORT IS FOR ONE (1) MODIFIED PROBE. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16064813 ↗
Other PROBE devices
- EXPEDIUM 279702030Depuy Spine, LLC · PROBE53 reports
- Sklar Instruments 94-5923Sklar Corporation · PROBE1 recall0 reports
- Sklar 96-2361Sklar Corporation · PROBE1 recall0 reports
- MOSS 275010140Depuy Spine, LLC · PROBE28 reports
- EXPEDIUM 279702040Depuy Spine, LLC · PROBE21 reports
- MULTILOC 03.019.029Synthes GmbH · PROBE15 reports
- MOSS 275010160Depuy Spine, LLC · PROBE11 reports
- EXPEDIUM 279702010Depuy Spine, LLC · PROBE9 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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