REF: 99-709245 recall
REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile
Why was REF: 99-709245 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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot # B4771336 and B4771337, UDI: 18059015373653
- Product
- REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile
- Recalling firm
- Orthofix Srl
- Quantity
- 2 units
- Distribution
- US: Unknown, OUS: Unknown
- Recall date
- June 25, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)