T2 ALPHA 2333-1036SRecalls & reported problems
Stryker GmbH · Femoral Nail GT, RIGHT · 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 07613327285994), received between Dec 26, 2022 and Mar 22, 2024 — 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
- Failure of Implant2
- Cancer1
- Nonunion/Delayed-union Bone Fracture1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 22, 2024Break; Fracture; Break; Fracture
AS REPORTED: "NAIL BROKEN OFF AT LAG SCREW HOLE. THE PATIENT HAS BONE TUMOR DUE TO BREAST CANCER, AND BONE FUSION IS NOT ORIGINALLY EXPECTED. THE FRACTURE OF THE IMPLANT IS UNAVOIDABLE, BUT THE FRACTURE OF THE PROPHYLACTIC IMPLANT HAS IMPAIRED THE FIXATION OF THE FRACTURE SITE, AND REVISION SURGERY IS PLANNED ON (B)(6) 2024."
Patient problems: Cancer; Failure of Implant
MAUDE report 18960421 ↗InjuryDec 26, 2022Break; Fracture; Break; Fracture
IT WAS REPORTED THAT A NAIL BROKE AND A REVISION SURGERY WAS PERFORMED. ADDITIONALLY A NONUNION WAS REPORTED.
Patient problems: Failure of Implant; Nonunion/Delayed-union Bone Fracture
MAUDE report 16048862 ↗
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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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