Ball Nose Guide Wire, Ø3.0mm x 900mm 0101-900SRecalls & reported problems
Advanced Orthopaedic Solutions, Inc. · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00848665000047), received between Apr 27, 2026 and Apr 27, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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.
Reports received per month
Most reported problems
Device problems
- Improper or Incorrect Procedure or Method1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 27, 2026Improper or Incorrect Procedure or Method
IT WAS REPORTED THAT AFTER THE INITIAL SURGERY ON (B)(6) 2026, A REVISION SURGERY WAS PERFORMED ON THE SAME DAY BECAUSE A LEFT TROCHANTERIC NAIL HAD BEEN MISTAKENLY IMPLANTED INSTEAD OF THE RIGHT TROCHANTERIC NAIL. THE REVISION SURGERY WAS FINISHED SUCCESSFULLY USING THE RIGHT TROCHANTERIC NAIL. IT WAS NOT NECESSARY TO SWITCH THE SURGICAL TECHNIQUE. UPDATE 15-APR-2026 - FURTHER INFORMATION WAS RECEIVED: THE DISTRIBUTOR REPORTED THAT THE LABEL OF THE DEVICE WAS CORRECT. THE INCIDENT WAS CAUSED BY AN ERROR AT THE HOSPITAL. NO X-RAYS ARE AVAILABLE. THE INITIAL SURGERY AND THE REVISION SURGERY WERE PERFORMED IN THE SAME HOSPITAL THROUGH THE SAME SURGEON.
Patient problems: Insufficient Information
MAUDE report 25002210 ↗
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- EXPRESSEW 214141Medos International Sàrl · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1,166 reports
- N/A 9560524Medtronic Sofamor Danek, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT866 reports
- INHANCE 6500-11-104Depuy (Ireland) · Orthopedic manual surgical instrument831 reports
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- R3 71364450Smith & Nephew, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT520 reports
- N/A 9561524Medtronic Sofamor Danek, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT494 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 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.
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