Geminus GEMINUS Hook PlateRecalls & reported problems
Skeletal Dynamics L.L.C. · Class 2 · Implant
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00841506101514), received between Jul 20, 2020 and May 20, 2026 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Lack of Effect1
Patient problems
- Foreign Body In Patient1
- Loss of fracture reduction1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 20, 2026Lack of Effect
THE VOLAR MARGINAL FRAGMENT WAS NOT ADEQUATELY REDUCED DURING IMPLANTATION OF A GEMINUS HOOK PLATE EXTENSION, REQUIRING REVISION SURGERY.
Patient problems: Loss of fracture reduction
MAUDE report 25236486 ↗MalfunctionJul 20, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
A SURGEON WILL BE REVISING THIS DISASSOCIATED HOOK PLATE FROM THE GEMINUS PLATING SYSTEM.
Patient problems: Foreign Body In Patient
MAUDE report 10299814 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.