CrossTIE™ Individual ImplantRecalls & reported problems
Crossroads Extremity Systems · Intraosseous Fixation Implant to aid in fixation of fractures, fusions, and osteotomies of the toes, such as hammertoe, claw toe, mallet toe and inter-digital fusions. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00850310006540), received between Sep 29, 2022 and Sep 29, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (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 18, 2026.
Most reported problems
Device problems
- Fracture2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2022Fracture; Fracture
IN THIS CASE A 2.5 MM CROSSTIE IMPLANT WAS INSERTED INTO THE PROXIMAL PHALANX. WHILE ATTEMPTING TO FLIP THE MIDDLE PHALANX ONTO THE IMPLANT, THE IMPLANT BROKE. THE IMPLANT WAS SUCCESSFULLY REMOVED AND CAUSED A MINIMAL DELAY IN SURGERY. ALSO IN THIS CASE, TWO ADDITIONAL IMPLANTS WERE OPENED BUT NOT USED BECAUSE THE DOCTOR DECIDED HE WANTED TO USE A 0 DEGREE IMPLANT RATHER THAN A 10 DEGREE. THERE WAS NO COMPLAINT OR MALFUNCTION INVOLVING THE TWO UNUSED 10 DEGREE IMPLANTS. BROKEN IMPLANT WAS REMOVED AND ANOTHER 0 DEGREE IMPLANT WAS SUCCESSFULLY USED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15501556 ↗MalfunctionSep 29, 2022Fracture; Fracture
A CROSSTIE IMPLANT WAS BROKEN WHILE TRYING TO INSERT THE IMPLANT. A CROSSTIE UNIVERSAL INSERTER WAS USED TO INSERT THE SUBJECT IMPLANT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15501478 ↗
Other Screw, Fixation, Bone devices
- NA 03.043.029Synthes GmbH · Screw, fixation, bone503 reports
- OSTEORAPTOR 72201995Smith & Nephew, Inc. · Screw, fixation, bone253 reports
- Control 360 SK12Treace Medical Concepts, Inc. · Screw, Fixation, Bone195 reports
- HEALIX PEEK ORTHOCORD 222205Medos International Sàrl · Screw, fixation, bone186 reports
- PRECICE® Bone Transport System STP3.5-400Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-225Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-300Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 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.
How reports and recalls are matched · Editorial policy · Report an error on this page