T2 ALPHA 2331-0000SRecalls & reported problems
Stryker GmbH · Set Screw GT · 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327343113), received between Sep 8, 2023 and Aug 6, 2024 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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.
Reports received per month
Most reported problems
Device problems
- Improper or Incorrect Procedure or Method1
- Malposition of Device1
- Positioning Failure1
Patient problems
- Hip Fracture1
- No Clinical Signs, Symptoms or Conditions1
- Perforation1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 6, 2024Positioning Failure; Improper or Incorrect Procedure or Method; Positioning Failure; Improper or Incorrect Procedure or Method
SET SCREW WAS MOVING FREELY EVEN WHEN IT WAS FULLY IN NAIL WITHOUT ANY RESISTANCE. SURGEON TAKE IT OUT AND PUT 0MM CAP AND FINISHED THE OPERATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19916360 ↗InjurySep 8, 2023Malposition of Device; Malposition of Device
AS REPORTED: "T2ALPHAGT WAS USED IN THE RECOM MODE ON (B)(6) 2023 FOR A SUBTROCHANTERIC FRACTURE OF THE FEMUR . AFTER SURGERY, DR CONFIRMED CUTOUT BY BOTH LAG SCREWS AT FEMORAL HEAD WHEN POSTOPERATIVE FOLLOW-UP. REMOVAL SURGERY WAS DONE AT (B)(6) 2023. THE DR FELT THAT THE SET SCREWS SEEMED TO BE LOOSELY FASTENED TO THE LAG SCREWS DURING REMOVAL SURGERY."
Patient problems: Hip Fracture; Perforation
MAUDE report 17714467 ↗
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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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