T2 1897-6090SRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04546540384782), received between Aug 13, 2018 and Mar 23, 2026 — classified as 3 injuries.

The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (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

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryMar 23, 2026Loosening of Implant Not Related to Bone-Ingrowth

  AS REPORTED: "THE LAG SCREW OF THE T2ALPHAGT WAS NOT SEATED WITHIN THE SCREW HOLE, RESULTING IN FEMORAL SHORTENING WHEN THE PATIENT APPLIED WEIGHT POSTOPERATIVELY, CAUSING THE PROXIMAL END OF THE NAIL TO PROTRUDE FROM THE FEMUR."

  Patient problems: Perforation

  MAUDE report 24670488 ↗
• InjuryApr 5, 2024Malposition of Device; Malposition of Device

  AS REPORTED: "THE SURGERY WAS PERFORMED ON (B)(6), BUT THE TWO PROXIMAL LAG SCREWS WERE INSERTED OFF THE NAIL. THE PROXIMAL BONE FRAGMENT SLID 7-8 CM DISTALLY, AND THE FEMUR HAS SHORTENED. REVISION SURGERY WAS PERFORMED ON (B)(6)."

  Patient problems: Failure of Implant; Unequal Limb Length

  MAUDE report 19055059 ↗
• InjuryAug 13, 2018Adverse Event Without Identified Device or Use Problem

  THE MANUFACTURER BECAME AWARE OF ADVERSE EVENTS FROM THE NORWEGIAN HIP FRACTURE REGISTER. THE TITLE OF THIS REPORT IS ¿T2 RECON IN THE NORWEGIAN HIP FRACTURE REGISTER¿ WHICH IS ASSOCIATED WITH THE T2 RECON NAILING SYSTEM, WITHIN THAT REPORT, POST-OPERATIVE COMPLICATIONS/ ADVERSE EVENTS WERE REPORTED, WHICH OCCURRED BETWEEN 2009 AND 2017. A REVIEW OF THE COMPLAINT HANDLING DATABASE REVEALED THAT THE EVENTS HAVE NOT BEEN REPORTED PREVIOUSLY TO STRYKER, THEREFORE 13 EVENTS WERE INITIATED RETROSPECTIVELY FOR DIFFERENT ADVERSE EVENTS MENTIONED IN THE REPORT. THIS PRODUCT INQUIRY ADDRESSES REVISION SURGERY DUE TO A NEW FRACTURE AROUND THE IMPLANT. THE PATIENT RECEIVED A RE-OSTEOSYNTHESIS.

  Patient problems: Bone Fracture(s)

  MAUDE report 7777998 ↗