Skip to content

Calibrate 326-07102205Recalls & reported problems

Alphatec Spine, Inc. · CALIBRATE CCX-S, 7 x 10 x 22mm 5° · Class 2 · Implant

All models of Calibrate (44)

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. Dec 15, 2024Open, Classified

    Complaints have been received regarding post-operative implant collapse.

    Z-1065-2025 · Root cause: Under Investigation by firm · 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