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Recall Observatory FDA recall evidence

Device product

Vantage Total Ankle Tibial Insert, Fixed Bearing, 10 mm, Left, Size 3. Exactech Inc. Intended for patients with ankle joints damage by severe rheumatoid, post-traumatic, or degenerative arthritis. It is also indicated for revision of failed previous reconstructions where sufficient bone stock and soft tissue integrity are present. Indicated for cemented use only.

Z-0201-2018

May 16, 2017

Class II

Product summary

Firm
Exactech, Inc.
Event
Event 77479
Status
Terminated
Classification
Class II
Quantity
9
Official record key
device-enforcement:Z-0201-2018

Official wording

Reason: Possible inner labeling and packaged device not matching the outer label on the box.

Code information: Catalog Number 350-21-43, Serial Range 4537323 - 4537331, Expiration August 2024

Distribution pattern: Distributed in North Carolina

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Possible inner labeling and packaged device not matching the outer label on the box.