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FORZA PTCRecalls & reported problems across all models

Orthofix US LLC · 76 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 PTC model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.

Adverse event reports
3
Deaths reported
0
Injuries reported
3
Recalls
1

We found 76 models of FORZA PTC by Orthofix US LLC in the FDA's device registry (GUDID). Together they are named in 3 adverse event reports in the FDA's MAUDE database, received between May 23, 2017 and Jul 14, 2017 — classified as 3 injuries.

The most frequently reported specific device problem is “Malposition of Device” (2 reports).

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 PTC 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-0892-2026 · Root cause: Device Design · names 76 of these models · Recall details · FDA record ↗

Most reported FORZA PTC problems

Device problems

  • Malposition of Device2
  • Migration or Expulsion of Device2
  • Material Protrusion/Extrusion1

Patient problems

  • No Known Impact Or Consequence To Patient2
  • Nerve Damage1

FORZA PTC models

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

Recent FORZA PTC adverse event reports

The 3 most recent reports across all models, in the reporter's own words as published by the FDA.

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