Skip to content

IMPIX MANTA B20181973Recalls & reported problems

Medicrea International · IMPIX-MANTA ON HOLDER MEDIUM 7mm - 3° · Class 2 · Implant

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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Jul 12, 2023Open, Classified

    There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.

    Z-2456-2023 · Root cause: Under Investigation by firm · FDA record ↗

Other Intervertebral Fusion Device With Bone Graft, Cervical devices

All Intervertebral Fusion Device With Bone Graft, Cervical devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.