Skip to content

FORZA Ti 38-2514SPRecalls & reported problems

Orthofix US LLC · 9W X 23L X 14H, 8° STRAIGHT, STERILE · Class 2 · Implant

All models of FORZA Ti (91)

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

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

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

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's 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, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Recalls naming this device

  1. Nov 3, 2025Open, Classified

    Labeling contains claims that are not consistently present.

    Z-0895-2026 · Root cause: Device Design · Recall details · FDA record ↗

Other Intervertebral fusion device with bone graft, lumbar devices

All Intervertebral fusion device with bone graft, lumbar devices →

Sources and updates

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