InjuryJDI
UNK Cup
Received Jul 31, 2026
Report 0001822565-2026-02729 · MDR key 50097189
Device
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
Unknown
- Insufficient Information
Narrative
Description of Event or Problem
It was reported that the patient is being considered for a hip revision to implant a custom triflange for unknown reasons. Attempts have been made and no further information has been provided.
Additional Manufacturer Narrative
(b)(4)The device will not be returned for analysis; however, an investigation of the reported event is in progress. Once the investigation is completed, a supplemental MedWatch 3500A will be submitted.