Skip to content

FORZA TiRecalls & reported problems across all models

Orthofix US LLC · 91 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names at least one FORZA Ti model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls
1

We found 91 models of FORZA Ti by Orthofix US LLC in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

1 FDA recall record name at least one of these models by its device identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

FORZA Ti recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

  1. Nov 3, 2025Open, Classified

    Labeling contains claims that are not consistently present.

    Z-0895-2026 · Root cause: Device Design · names 91 of these models · Recall details · FDA record ↗

FORZA Ti models

91 models, most reported first. Each model has its own page with its reports, recalls and device details.

Other Orthofix US LLC products

All Orthofix US LLC devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page