Symmetry Hardy 80-1345Recalls & reported problems
Aspen Surgical Products, Inc. · Symmetry® Curette, Hardy, Angled Down, 3 mm Tip Width, 4 3/4 in Working Length, 9 1/4 in · Class 1
Data updated Oct 18, 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 00887482030707), received between Jul 10, 2025 and Jul 10, 2025 — 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 10, 2025Break; Break
COMPLAINANT ALLEGES "A 55-YEAR-OLD FEMALE PATIENT WAS TREATED FOR ENDONASAL EXCISION OF A PITUITARY MICROADENOMA IN THE CONTEXT OF CUSHING'S DISEASE. THE CURETTE USED TO REMOVE PART OF THE PITUITARY ADENOMA BROKE INSIDE THE PATIENT'S NASAL CAVITY. THE SURGEON WAS ABLE TO RETRIEVE THE PIECE, WITH DIFFICULTY."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22469550 ↗
Other Curette, Surgical, General Use devices
- Sklar Instruments 941-1320Sklar Corporation · CURETTE, SURGICAL, GENERAL USE1 recall0 reports
- Medtronic Reusable Instruments 2900163Medtronic Sofamor Danek, Inc. · CURETTE, SURGICAL, GENERAL USE11 reports
- Medtronic Reusable Instruments 9560547Medtronic Sofamor Danek, Inc. · CURETTE, SURGICAL, GENERAL USE7 reports
- na 2900162Medtronic Sofamor Danek, Inc. · CURETTE, SURGICAL, GENERAL USE3 reports
- Medtronic Reusable Instruments 907347Medtronic Sofamor Danek, Inc. · CURETTE, SURGICAL, GENERAL USE3 reports
- Medtronic Reusable Instruments 875-304Medtronic Sofamor Danek, Inc. · CURETTE, SURGICAL, GENERAL USE2 reports
- na 907349Medtronic Sofamor Danek, Inc. · CURETTE, SURGICAL, GENERAL USE1 report
- Medtronic Reusable Instruments 9560546Medtronic Sofamor Danek, Inc. · CURETTE, SURGICAL, GENERAL USE1 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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