Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
REF: 99-709245 Recalled by Orthofix Srl Due to Retrospective; Their is the potential that implantable intramedullary...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Orthofix Srl directly.
Affected Products
REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile
Quantity: 2 units
Why Was This Recalled?
Retrospective; Their is the potential that implantable intramedullary lengthening nails may bend at the distal tail during insertion resulting in having to be replaced.
Where Was This Sold?
US: Unknown, OUS: Unknown
About Orthofix Srl
Orthofix Srl has 34 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report