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Vantage 350-01-03Recalls & reported problems

Exactech, Inc. · Class 2 · Implant

All models of Vantage (66)

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885862276711), received between Apr 6, 2023 and Apr 6, 2023 — classified as 1 injury.

6 other recalls cover devices cleared under the same FDA submission (K152217); they may or may not involve this specific model.

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.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1
  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Pain1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 6, 2023Adverse Event Without Identified Device or Use Problem; Appropriate Device Problem Term/Code Not Available; Adverse Event Without Identified Device or Use Problem; Appropriate Device Problem Term/Code Not Available

    IT WAS REPORTED VIA CLINICAL STUDY, THAT THE 76 YO MALE PATIENT WAS EXPERIENCING INCREASING LEFT ANKLE PAIN. THE RESULTS OF THE CT SCAN SHOWED HE NEEDED A NEW TALAR COMPONENT AND ST (SUBTALAR) ARTHRODESIS. THE DATE OF ADVERSE EVENT ONSET IS (B)(6) 2022. THE PATIENT¿S OUTCOME WAS LAST KNOWN AS RESOLVED WITH A REVISION ON (B)(6) 2022.

    Patient problems: Pain

    MAUDE report 16694854 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K152217. One submission often covers many models, so check the product and lot details in each record.

  • Z-0587-2024 · Nov 21, 2023 · Open, Classified
    Exactech Vantage Ankle System, Catalog Numbers: a) 350-21-04, b) 350-22-03
  • Z-0024-2022 · Aug 30, 2021 · Open, Classified
    Vantage Total Ankle System including a. Vantage Fixed-Bearing Polyethylene Liner Component (Product Line: 350-21-XX, 350-22-XX); b. Vantage Mobile-Bearing Polyethylene Line
  • Z-2926-2020 · Aug 10, 2020 · Open, Classified
    The Vantage Total Ankle Tibial Insert, Fixed Bearing, Size 4, Right 10mm.
  • Z-2966-2018 · Jul 13, 2018 · Terminated
    Tibial Alignment Guide, REF 351-10-00 Vantage Fixed Ankle system components for ankle replacements.
  • Z-0201-2018 · May 16, 2017 · Terminated
    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 degene
  • Z-0200-2018 · May 16, 2017 · Terminated
    Vantage Total Ankle Tibial Insert, Fixed Bearing, 7 mm, Left, Size 3. Exactech Inc., Intended for patients with ankle joints damage by severe rheumatoid, post-traumatic, or dege

Other Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer devices

All Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer devices →

Sources and updates

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