MotoBAND Implant, 3.5mm x 38mm Anti-Drift Bolt, Fully ThreadedRecalls & reported problems
Crossroads Extremity Systems · The MotoBAND™ CP Implant System is a bone plating system indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of plates and screws. · Class 2 · Implant
Data updated Oct 18, 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 00815432029587), received between Nov 3, 2022 and Jan 17, 2025 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break1
- Entrapment of Device1
- Migration1
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 17, 2025Break; Entrapment of Device; Break; Entrapment of Device
UPDATED EVENT DESCRIPTION: IT WAS REPORTED THAT ON (B)(6) 2023, THE PATIENT PRESENTED PAINFUL BUNION DEFORMITY ON THE LEFT FOOT. ON (B)(6) 2023, THE PATIENT UNDERWENT LAPIDUS BUNIONECTOMY VIA FIRST METATARSOCUNEIFORM ARTHRODESIS WITH AKIN OSTEOTOMY. ON (B)(6) 2024, THE PATIENT EXPERIENCED LEFT MIDFOOT PAIN. X-RAYS WERE TAKEN AND IT WAS DISCOVERED THAT THE ANTIDRAFT BOLT PLACED ON HER INITIAL SURGERY IN 2023 HAD BROKEN WITH A PIECE OF THE SCREW EMBEDDED INTO THE BASE OF THE SECOND METATARSAL. ON (B)(6) 2024, THE PATIENT UNDERWENT A REMOVAL SURGERY DUE TO MECHANICAL BREAKDOWN OF INTERNAL FIXATION DEVICE OF BONES OF FOOT. DOI: (B)(6) 2023, DOR: (B)(6) 2024, LEFT FOOT.
Patient problems: Foreign Body In Patient; Pain
MAUDE report 21178098 ↗MalfunctionNov 3, 2022Migration; Migration
THE REPORTER STATES THAT THE ANTI-DRIFT BOLT WAS REMOVED BY THE SURGEON APPROXIMATELY 3 MONTHS AFTER THE INITIAL PROCEDURE. NO PAIN OR SYMPTOMS WERE REPORTED WITH THE SCREW MIGRATION. THE JOINT WAS FUSED. THE ANTI-DRIFT BOLT WAS REMOVED, AND THE PATIENT RETURNED TO FULL ACTIVITY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15723613 ↗
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- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-MLT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-MRT42Nuvasive Specialized Orthopedics, Inc. · Plate, 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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