CrossTIE™ 1443-2510Recalls & reported problems
Crossroads Extremity Systems · The CrossTie™ Intraosseous Fixation System is used to aid in the fixation of fractures, fusions, and osteotomies of the toes, including 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
- 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 00850310006533), received between Sep 29, 2022 and Sep 29, 2022 — classified as 1 malfunction.
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
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2022Fracture; Fracture
THE DOCTOR WAS HAVING TROUBLE GETTING THE IMPLANT TO RELEASE FROM THE OLD INSERTER BECAUSE IT WAS REALLY TIGHT. ONCE THE DOCTOR WAS FINALLY ABLE TO RELEASE THE IMPLANT, THE IMPLANT BROKE IN THE PROCESS. THE DOCTOR THEN OPENED ANOTHER CROSSTIE KIT AND BEGAN TO INSERT THE IMPLANT. WHILE HE WAS INSERTING THE IMPLANT, THE DOCTOR NOTICED A CRACK IN THE CORTEX. ONCE THE DOCTOR HAD NOTICED THAT THE CORTEX WAS CRACKED, HE DECIDED TO USE A K-WIRE INSTEAD OF A CROSSTIE. HE DID NOT DIRECTLY ADDRESS THE CRACK THAT OCCURRED. OTHER CROSSTIE IMPLANTS WERE SUCCESSFULLY IMPLANTED BY THIS DOC DURING THIS PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15501740 ↗
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.
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