T2 ALPHA 2331-1036SRecalls & reported problems
Stryker GmbH · Femoral Nail GT, LEFT · Class 2 · Implant
All models of T2 ALPHA (123)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327289367), received between Jul 17, 2023 and Jul 22, 2025 — classified as 2 injuries.
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break2
- Fracture2
Patient problems
- Bone Fracture(s)1
- Failure of Implant1
- Implant Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJul 22, 2025Break; Fracture; Break; Fracture
AS REPORTED: "PRIMARY SURGERY WITH T2A-GT WAS PERFORMED ON A PATIENT WITH A FEMORAL TROCHANTERIC FRACTURE ON (B)(6) 2024. THE PATIENT WAS ADMITTED AGAIN BECAUSE OF A NAIL FRACTURE ON (B)(6) 2025. A REVISION SURGERY IS SCHEDULED ON (B)(6) 2025 TO INSERT A T2A-PF NAIL AFTER REMOVAL OF THE FRACTURED NAIL."
Patient problems: Bone Fracture(s)
MAUDE report 22564801 ↗InjuryJul 17, 2023Break; Fracture; Break; Fracture
AS REPORTED: "NAIL BREAKAGE WAS OBSERVED AT THE MOST PROXIMAL SCREW HOLE OF THE DISTAL PART. THE NAIL WILL BE REMOVED AND REVISION SURGERY IS SCHEDULED ON (B)(6) WITH A RETROGRADE NAIL." IT WAS ADDITIONALLY REPORTED THAT THE PATIENT EXPERIENCE PAIN.
Patient problems: Failure of Implant; Implant Pain
MAUDE report 17334869 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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