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[Recalled] REF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile — Retrospective | FDA 2024-09-24

recall fda device italy

Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.

Recall details

ProductREF: 99-709245, Fitbone Trochanteric Nail L245mm, D9mm, Sterile
Brand / manufacturerOrthofix Srl
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1977-2025
Country of noticeItaly
Risk levelClass II
Hazard typerecall
Notice date24 September 2024
EAN / barcode18059015373653

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.

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