T2 1843-1134SRecalls & reported problems
Stryker GmbH · Reconstruction Nail R1.5, Ti, LEFT · Class 2 · Implant
Data updated Oct 18, 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 04546540383839), received between Feb 27, 2019 and Feb 27, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (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
- Fracture1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 27, 2019Fracture
IT WAS REPORTED THAT SECONDARY FRACTURE OCCURRED AROUND THE DISTAL LATERAL SCREW OF T2 NAIL ON (B)(6) 2018. DURING REHABILITATION, COMPLAINED A PAIN AROUND THE KNEE ALTHOUGH CONTINUED REHABILITATION. THEN VISITED A HOSPITAL AND FOUND A SECONDARY FRACTURE IN THE NAIL DISTAL. IT WILL REVISION SURGERY ON (B)(6) 2019.
Patient problems: Pain
MAUDE report 8374915 ↗
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- TRIGEN 71674067Smith & Nephew, Inc. · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES201 reports
- PRECICE Intramedullary Limb Lengthening System LSB5-040Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
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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