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, ClassifiedExactech Vantage Ankle System, Catalog Numbers: a) 350-21-04, b) 350-22-03
- Z-0024-2022 · Aug 30, 2021 · Open, ClassifiedVantage 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, ClassifiedThe Vantage Total Ankle Tibial Insert, Fixed Bearing, Size 4, Right 10mm.
- Z-2966-2018 · Jul 13, 2018 · TerminatedTibial Alignment Guide, REF 351-10-00 Vantage Fixed Ankle system components for ankle replacements.
- Z-0201-2018 · May 16, 2017 · TerminatedVantage 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 · TerminatedVantage 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
- Vantage 350-22-03Exactech, Inc. · Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer2 recalls2 reports
- Vantage 350-21-04Exactech, Inc. · Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer2 recalls0 reports
- INFINITY 33630023Wright Medical Technology, Inc. · PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER60 reports
- INFINITY 33600020Wright Medical Technology, Inc. · PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall9 reports
- Vantage 350-22-02Exactech, Inc. · Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer1 recall5 reports
- INFINITY 33650003Wright Medical Technology, Inc. · PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER55 reports
- INFINITY 33630022Wright Medical Technology, Inc. · PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER54 reports
- INFINITY 33600030Wright Medical Technology, Inc. · PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall4 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page