INFINITY™ EVERLAST™ 33685508Recalls & reported problems
Wright Medical Technology, Inc. · Class 2 · Implant
All models of INFINITY EVERLAST (20)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889797074681), received between Oct 11, 2024 and Sep 23, 2026 — classified as 3 injuries.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem3
Patient problems
- Numbness2
- Neuralgia1
- Pain1
- Wound Dehiscence1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjurySep 23, 2026Adverse Event Without Identified Device or Use Problem
Study: Stryker ITAR-2.Site: (b)(6).Subject: (b)(6).Painful right total ankle replacement, four and a half years post-implantation with associated ankle pain, burning sensation, and increased numbness dorsally to the great toe.Procedure Related :Yes.Device Related: No.
Patient problems: Neuralgia; Numbness; Pain
MAUDE report 50865168 ↗InjuryOct 21, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
SUBJECT: (B)(6) INFINITY WITH ADAPTIS ANKLE (ITAR-2) STUDY. ON (B)(6) 2021 PATIENT NOTICED NUMBNESS IN LATERAL ASPECT OF RIGHT FOOT ABOUT 2 MONTHS AFTER OPERATION. NO PAIN WAS REPORTED. THE NUMBNESS IS REPORTED ON THE OPERATIVE ANKLE. ADDITIONALLY, SEVERAL AE UPDATES WERE PROVIDED. AE UPDATE 1 (B)(6) 2022: PATIENT REPORTS NO PAIN BUT HAS NUMBNESS AND A STINGING SENSATION IN FOOT AFTER PROLONGED WALKING. AE UPDATE 2 (B)(6) 2023: NUMBNESS STILL REPORTED 30-SEP-2025: AFTER REVIEW BY THE MEDICAL EXPERT THIS AE WAS QUERIED TO DETERMINE IF IT WAS PROCEDURE RELATED DUE TO PROXIMITY TO THE SURGERY. THE STUDY COORDINATOR REPLIED AFTER CONFIRMING WITH THE PI THAT THE NUMBNESS WAS PROCEDURE RELATED DUE TO ANESTHESIA BLOCK.
Patient problems: Numbness
MAUDE report 23347798 ↗InjuryOct 11, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
AS REPORTED: "SUBJECT: (B)(6) INFINITY¿ WITH ADAPTIS¿ TOTAL ANKLE REPLACEMENT FOLLOW-UP (ITAR2). (B)(6) 2022: DELAYED WOUND HEALING. SMALL OPEN WOUND NOTED. PATIENT REFERRED TO WOUND CARE MANAGEMENT. (B)(6) 2022: IMPROVING. SLIGHT REDNESS THAT IS HEALING. (B)(6) 2022: RESOLVED. CLEAN, DRY, AND INTACT WITHOUT SIGNS OF INFECTION."
Patient problems: Wound Dehiscence
MAUDE report 20426074 ↗
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.
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