UNKNOWN VISION RINGLOC ACETABULAR SHELL
Received Jul 14, 2026 · Event occurred Jul 29, 2024
Report 0001825034-2026-02059 · MDR key 25813856
Device
Generic name
Prosthesis, Hip
Manufacturer
Zimmer Biomet, Inc.Catalog number
UNK VISION RINGLOC SHELL
Lot number
UNKNOWN
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Male
- Insufficient Information
Narrative
Description of Event or Problem
IT WAS REPORTED BY PATIENTS¿ LEGAL COUNSEL THAT THE PATIENT UNDERWENT A RIGHT HIP REVISION PROCEDURE APPROXIMATELY NINE YEARS POST-IMPLANTATION DUE TO UNKNOWN REASONS. IT WAS CONFIRMED THAT NO FURTHER INFORMATION COULD BE PROVIDED.
Additional Manufacturer Narrative
(B)(4). D10: UNKNOWN RINGLOC ACETABULAR LINER. UNKNOWN MODULAR TAPERLOC FEMORAL POROUS COATED. UNKNOWN MODULAR HEAD. NO PRODUCT WAS RETURNED OR PICTURES PROVIDED; VISUAL AND DIMENSIONAL EVALUATIONS COULD NOT BE PERFORMED. DEVICE HISTORY RECORD REVIEW CANNOT BE PERFORMED WITHOUT PRODUCT IDENTIFICATION. MEDICAL RECORDS WERE NOT PROVIDED. A DEFINITIVE ROOT CAUSE CANNOT BE DETERMINED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR TRENDS.