Class II
Medical Device Recall: REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile
Orthofix Srl · September 24, 2024
Reason for Recall
Retrospective; Their is the potential that implantable intramedullary lengthening nails may bend at the distal tail during insertion resulting in having to be replaced.
Distribution
US: Unknown, OUS: Unknown
Quantity Affected
2 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1977-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.