[Recalled] REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile — Retrospective | FDA 2024-09-24
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile |
|---|---|
| Brand / manufacturer | Orthofix Srl |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1977-2025 |
| Country of notice | Italy |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 24 September 2024 |
| EAN / barcode | 18059015373653 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Retrospective; Their is the potential that implantable intramedullary lengthening nails may bend at the distal tail during insertion resulting in having to be replaced.
This Class II recall concerns device products distributed in Italy and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Orthofix Srl
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.