T2 ALPHA 2331-1242SRecalls & 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
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327284461), received between Jun 10, 2020 and Jun 10, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Separation Problem” (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
- Separation Problem1
Patient problems
- Failure of Implant1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 10, 2020Separation Problem; Separation Problem
THE REPRESENTATIVE WAS PROVIDED A PICTURE OF AN X-RAY SHOWING A T2 ALPHA GREATER TROCH NAIL WITH THE DISTAL LOCKING SCREW BACKING OUT. SURGEON'S TEXT STATES: "WHY IS IT THAT THE LOCKING DISTAL SCREWS BACKED OUT BUT THE REGULAR SCREW DID NOT?" NO REVISION WAS REPORTED FOR THE PATIENT AT THIS TIME.
Patient problems: Failure of Implant; No Known Impact Or Consequence To Patient
MAUDE report 10140067 ↗
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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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