Vantage 350-10-02Recalls & reported problems
Exactech, Inc. · Class 2 · Implant
All models of Vantage (66)
Data updated Oct 18, 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 10885862302007), received between Nov 2, 2023 and Nov 2, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (1 report).
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture1
- Structural Problem1
Patient problems
- Failure of Implant1
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 2, 2023Fracture; Structural Problem; Fracture; Structural Problem
AS REPORTED, APPROXIMATELY 2.5 YEARS POST OP INITIAL LEFT ANKLE REPLACEMENT, THIS 56 Y/O FEMALE PATIENT WAS REVISED DUE THE LOCKING CLIP DISASSOCIATED FROM TIBIAL TRAY. CLIP BROKE IN SITU. SURGEON SWAPPED OUT CLIP & POLY. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. NO IMAGES OR X-RAYS AVAILABLE.
Patient problems: Failure of Implant; Insufficient Information
MAUDE report 18060431 ↗
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 Liner Co
- 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
- Vantage 350-21-02Exactech, 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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