Latitude™ - Elbow DKY122Recalls & reported problems
Tornier, Inc. · Ulnar Bushing · Class 2 · Implant
All models of Latitude - Elbow (35)
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 00846832010998), received between Oct 17, 2023 and Oct 17, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).
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
- Device Dislodged or Dislocated1
Patient problems
- Joint Dislocation1
- Joint Laxity1
- Numbness1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 17, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
AS REPORTED: "POST-OPERATIVE COMPLICATIONS SURFACED EIGHT DAYS FOLLOWING THE INITIAL SURGERY INVOLVING THE LATITUDE EV IMPLANT. THE PATIENT HAD ELBOW DISLOCATION, SIGNIFYING SIGNIFICANT INSTABILITY IN THE JOINT. THE PATIENT PRESENTED AT THE A&E WITH INTERMITTENT DISLOCATIONS AND REPORTED SENSATIONS OF PINS AND NEEDLES IN THE AFFECTED AREA. THE SURGEON CONFIRMED A CAUSAL RELATIONSHIP BETWEEN THESE COMPLICATIONS AND THE IMPLANTATION SURGERY. TO ADDRESS THE ISSUES, A REVISION SURGERY WAS DEEMED NECESSARY TO REPOSITION THE ULNAR CAP. THE RE-OPERATION TOOK PLACE ON (B)(6) 2023." UPDATE ON (B)(6) 2023 THE OPERATED ELBOW WAS THE RIGHT. HAND DOMINANCE = OPERATED.
Patient problems: Joint Dislocation; Joint Laxity; Numbness
MAUDE report 17952679 ↗
Other PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED devices
- DJO SURGICAL 540-00-000Encore Medical, L.P. · PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED64 reports
- Arcos Modular Revision Hip System 11-301321Biomet Orthopedics, LLC · PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED1 recall7 reports
- DJO SURGICAL 540-01-001Encore Medical, L.P. · PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED55 reports
- Arcos Modular Revision Hip System 11-301302Biomet Orthopedics, LLC · PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED1 recall5 reports
- Arcos Modular Revision Hip System 11-301343Biomet Orthopedics, LLC · PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED1 recall1 report
- ARROW IPN037140Teleflex Incorporated · PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED1 recall0 reports
- Comprehensive® SRS / Discovery® 211251Biomet Orthopedics, LLC · PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED1 recall0 reports
- Arcos Modular Revision Hip System 11-301325Biomet Orthopedics, LLC · PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED1 recall0 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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