INFINITY™ EVERLAST™ 33682208Recalls & 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
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889797074445), received between Oct 11, 2024 and Dec 22, 2025 — classified as 4 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 Problem4
Patient problems
- Pain2
- Ambulation or Postural Difficulties1
- Bone Fracture(s)1
- Deformity/ Disfigurement1
- Fall1
- Implant Pain1
- Joint Impingement1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryDec 22, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE STRYKER PROPHECY TEAM HAS RECEIVED A CT SCAN FOR UPCOMING REVISION SURGERY DUE TO ANKLE VARUS WITH HINDFOOT PAIN AND PAIN WITH WALKING.
Patient problems: Ambulation or Postural Difficulties; Deformity/ Disfigurement; Fall; Pain
MAUDE report 23864620 ↗InjurySep 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
STUDY: (B)(6). SUBJECT: (B)(6). (B)(6) 2024: PI REVIEWED HER SPECT/CT SCAN WITH HER TODAY, AND PI FEELS THAT HER IMAGES ARE MOST CONSISTENT WITH LATERAL GUTTER IMPINGEMENT. THIS IS ALSO CONCORDANT WITH HER EXAM AND FOCAL PAIN IN THE LATERAL GUTTER. PATIENT ELECTED TO PROCEED WITH A GUTTER DEBRIDEMENT. TREATMENT FOR THIS CONDITION WOULD CONSIST OF A LATERAL GUTTER DEBRIDEMENT. (B)(6) 2024: PATIENT HAD SURGERY ON THIS DAY FOR A RIGHT ANKLE ARTHROTOMY AND BONY DEBRIDEMENT OF LATERAL GUTTER.
Patient problems: Joint Impingement; Pain
MAUDE report 22963663 ↗InjuryOct 11, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
AS REPORTED: "SUBJECT: 200-003INFINITY¿ WITH ADAPTIS¿ TOTAL ANKLE REPLACEMENT FOLLOW-UP (ITAR2) (B)(6) 2021: PERSISTENT PAIN. PATIENT STATES SHE IS HAVING SIGNIFICANT PAIN ON THE MEDIAL ASPECT OF HER ANKLE. (B)(6) 2022: RESOLVED. DENIES PAIN AT OFFICE VISIT."
Patient problems: Implant Pain
MAUDE report 20426124 ↗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) 2021: INTRA-OPERATIVE FRACTURE (R LATERAL DISTAL TIBIAL FX). AFTER MAKING TIBIAL CUT, A FRACTURE WAS NOTED IN R LAT DISTAL TIBIA-NON-DISPLACED. NO ADDITIONAL PROCEDURES OR FIXATION WAS NEEDED. COMPONENTS WERE STABLE, ANKLE WAS STABLE AT END OF PROCEDURE.".
Patient problems: Bone Fracture(s)
MAUDE report 20426072 ↗
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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