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T2 ALPHA 2335-0936SRecalls & reported problems

Stryker GmbH · Femoral Nail PF, LEFT · Class 2 · Implant

All models of T2 ALPHA (123)

Data updated Oct 16, 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 07613327285635), received between Jan 12, 2023 and Jan 12, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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 16, 2026.

Most reported problems

Device problems

  • Break1
  • Fracture1

Patient problems

  • Ambulation or Postural Difficulties1
  • Failure of Implant1
  • Implant Pain1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJan 12, 2023Break; Fracture; Break; Fracture

    IT WAS REPORTED THAT A SUBTROCHANTERIC PROXIMAL FEMUR FRACTURE WAS TREATED WITH A T2 ALPHA PF NAIL. 5 WEEKS POST OP THE PATIENT REPORTS THAT AS SHE WAS WALKING AROUND HER HOME, SHE FELT AND HEARD A POP AND HER LEFT LEG GAVE OUT AND SHE WAS UNABLE TO AMBULATE AND HAD SEVERE PAIN. SHE HAD A REVISION SURGERY TO REMOVE THE BROKEN NAIL AND IT WAS REPLACED WITH A DEPUY SYNTHES 95 DEGREE BLADE PLATE WITH CORTICAL AND LOCKING SCREWS.

    Patient problems: Ambulation or Postural Difficulties; Failure of Implant; Implant Pain

    MAUDE report 16147214 ↗

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Sources and updates

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