MiniBunion™ MiniBunion, Non-Locking Screw, 2.7mm x 14mm - SterileRecalls & reported problems
Crossroads Extremity Systems · The MiniBunion™ Implant System is indicated for stabilization and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. It consist of an intramedullary implant and screws. · Class 2 · Implant
All models of MiniBunion (7)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00815432027019), received between May 24, 2023 and May 24, 2023 — classified as 2 injuries.
The most frequently reported specific device problem is “Migration” (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
- Migration2
Patient problems
- Failure of Implant2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 24, 2023Migration; Migration
IT WAS REPORTED THAT ON (B)(6)2023, THE OBLIQUE NON-LOCKING SCREW BACKED OUT. SURGEON REMOVED THE OBLIQUE SCREW. BUNION CORRECTION IS GOOD. THIS REPORT IS FOR ONE (1) MINIBUNION NONLCKNG SCR 2.7MMX14MM STER. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: Failure of Implant
MAUDE report 16991960 ↗InjuryMay 24, 2023Migration; Migration
IT WAS REPORTED THAT ON (B)(6) 2022, THE PATIENT UNDERWENT SURGERY TO IMPLANT THE MINIBUNION IMPLANTS. ON (B)(6) 2023, THE OBLIQUE NON-LOCKING SCREW BACKED OUT POSTOPERATIVELY, REQUIRING A SURGERY TO REMOVE THE SCREW. BUNION CORRECTION WAS GOOD. THE IMPLANT HAD BEEN IN THE PATIENT FOR GREATER THAN 12 MONTHS. THIS REPORT INVOLVES ONE MINIBUNION, NON-LOCKING SCREW, 2.7MM X 14MM - STERILE. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: Failure of Implant
MAUDE report 16991247 ↗
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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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