Orthofix Srl 2025-06-25 Health serious FDA
Health · FDA · Recall #FDA-Z-1977-2025
REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile Recall
Issued June 25, 2025 · Orthofix Srl
In June 2025, Orthofix Srl recalled the REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Retrospective; Their is the potential that implantable intramedullary lengthening nails may bend at the distal tail during insertion resulting in having to be replaced.
What you should do
- 1 Stop using REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Orthofix Srl to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Orthofix Srl
- Category
- Health
- Recall date
- June 25, 2025
- Units affected
- Not reported
- Sold at
- US: Unknown, OUS: Unknown
- Recall number
- FDA-Z-1977-2025
- Made in
- Italy
- Issuing agency
- FDA
In context
- Orthofix Srl has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.