T2 ALPHA 2331-1244SRecalls & reported problems
Stryker GmbH · Femoral Nail GT, LEFT · Class 2 · Implant
All models of T2 ALPHA (123)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327284355), received between Jul 14, 2021 and Jul 14, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (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.
Most reported problems
Device problems
- Fracture1
Patient problems
- Discomfort1
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 14, 2021Fracture; Fracture
IT WAS REPORTED THE PATIENT HAD PREVIOUS SURGERY (B)(6) 2021 FOR A LEFT PROXIMAL FEMUR FRACTURE THAT WAS TREATED WITH A T2 ALPHA RECON NAIL. AFTER 3 MONTHS THE NAILED FAILED AT THE INFERIOR RECON SCREW HOLE. PATIENT TOLD THE SURGEON THAT SHE HAD ONLY BEEN DOING PT WHEN SHE FELT SOMETHING UNCOMFORTABLE IN HER LEFT HIP. X-RAY CONFIRMED THAT THE IMPLANT HAD FAILED. ON (B)(6) 2021 THE BROKEN T2 ALPHA RECON NAIL WAS REMOVED AND REVISED WITH A SYNTHES TFNA.
Patient problems: Discomfort; Failure of Implant
MAUDE report 12169625 ↗
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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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