Symmetry Verity™ 80-1531Recalls & reported problems
Aspen Surgical Products, Inc. · Verity Hook, Nerve, Titanium Handle, 3.0 mm Ball Tip, Stainless Steel Shaft, 7 1/4 in · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887482031070), received between Dec 29, 2025 and Feb 24, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (2 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. 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
- Break2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 24, 2026Break
COMPLAINANT ALLEGES "I HAVE A CUSTOMER (B)(6) IFS- (B)(6) THAT IS REQUESTING A QUALITY REVIEW FOR TWO INSTRUMENTS THAT THEY HAVE HAD THAT ARE REPORTED TO HAVE BROKEN DURING A PROCEDURE. NO PATIENTS WERE HARMED, BUT THE SAME CATALOG NUMBER HAS BROKEN TWICE, SO THEY WANTED US TO LOOK INTO IT."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24430711 ↗MalfunctionDec 29, 2025Break; Break
COMPLAINANT ALLEGES "THE TIP OF A MICRO "L" HOOK INSTRUMENT BROKE DURING THE PROCEDURE. A MAGNET JUST USED TO TRY TO FIND IT IN THE PATIENT. ROLLING MAGNETS WERE USED TO SEARCH THE FLOOR AND BACK TABLE. ALL SPONGES AND LAPS WERE SEARCHED. DRAPES WERE SEARCHED AFTER TAKEN OFF PATIENT AS WELL. MACHINE AND HE SAID THAT WAS NOT AN OPTION."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23908466 ↗
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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 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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