Symmetry Verity™ 58-6063TRecalls & reported problems
Aspen Surgical Products, Inc. · Verity Hook, Nerve, Ball Tip, Titanium Handle, 3.0 mm, 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 00887482103654), received between Feb 22, 2023 and Feb 22, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Fragmentation” (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.
Most reported problems
Device problems
- Material Fragmentation2
Patient problems
- Foreign Body In Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 22, 2023Material Fragmentation; Material Fragmentation
DURING AN ANTERIOR CERVICAL DISECTOMY THE BALL TIP OF THE NERVE HOOK BROKE OFF. THEY NOTICED THE DAMAGED NERVE HOOK AFTER THE PROCEDURE AND SENT THE PATIENT IT IMAGING. THE IMAGING CONFIRMED THAT THAT THE BALL TIP REMAINED THE PATIENT. THE DOCTOR DETERMINED THAT AN ADDITIONAL SURGERY WAS NOT NECESSARY TO REMOVE THE TIP.
Patient problems: Foreign Body In Patient
MAUDE report 16421972 ↗MalfunctionFeb 22, 2023Material Fragmentation; Material Fragmentation
THE CUSTOMER ALLEGED THAT DURING A SECOND ANTERIOR CERVICAL DISECTOMY THE BALL TIP OF THE NERVE HOOK BROKE OFF. THEY NOTICED THE DAMAGED NERVE HOOK AFTER THE PROCEDURE AND SENT THE PATIENT IT IMAGING. THE IMAGING CONFIRMED THAT THAT THE BALL TIP REMAINED THE PATIENT. THE DOCTOR DETERMINED THAT AN ADDITIONAL SURGERY WAS NOT NECESSARY TO REMOVE THE TIP.
Patient problems: Foreign Body In Patient
MAUDE report 16421930 ↗
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- Centurion I68655Centurion Medical Products Corporation · HOOK, SURGICAL, GENERAL & PLASTIC SURGERY1 recall0 reports
- Centurion 67810Centurion Medical Products Corporation · HOOK, SURGICAL, GENERAL & PLASTIC SURGERY1 recall0 reports
- Centurion I68785Centurion Medical Products Corporation · HOOK, SURGICAL, GENERAL & PLASTIC SURGERY1 recall0 reports
- Centurion 66660Centurion Medical Products Corporation · HOOK, SURGICAL, GENERAL & PLASTIC SURGERY1 recall0 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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