FDA Adverse Event Injury Summary report: N

NV GXL LINER NEUTRAL, 36MM ID, GROUP 2 CUPS

MDR report key: 24643075 · Received March 19, 2026

Report

Report Number
1038671-2026-00302
Event Type
Injury
Date Received
March 19, 2026
Date of Event
March 4, 2026
Report Date
March 19, 2026
Manufacturer
EXACTECH, INC.
Product Code
JDI
UDI-DI
10885862207081
PMA / PMN Number
K121392
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SP
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

D10: 01-032-03-3600 - UNIV.CUP CABEZA CERAM. DELTA 36 +0 21021267/033. 164-01-09 - VASTAGO ELEMENT S/COLLAR OFFSET STD. Nº9 6619931. 180-11-52 - (DISC) NOVATION CROWN CU P, CLUSTER-HOLE WITH HA, 6689744. THE REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. NO DEVICE WAS RETURNED FOR EVALUATION; FURTHER, PHOTOGRAPHS AND/OR RADIOGRAPH IMAGES WERE NOT PROVIDED FOR REVIEW. OPERATIVE NOTES AND/OR MEDICAL RECORDS WERE NOT PROVIDED FOR REVIEW OF USAGE/TECHNIQUE. A DEFINITIVE ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT PROVIDED. IF ANY FURTHER INFORMATION IS OBTAINED THAT WOULD CHANGE OR ALTER ANY INFORMATION PROVIDED, A SUPPLEMENTAL REPORT WILL BE FILED ACCORDINGLY.

Description of Event or Problem · 0

AS REPORTED, A PATIENT UNDERWENT AN INITIAL TOTAL HIP ARTHROPLASTY, ON THE RIGHT SIDE. SUBSEQUENTLY, THE PATIENT WAS DIAGNOSED WITH EARLY WEAR OF THE PROSTHETIC POLYETHYLENE WITH PARTICULATE DISEASE, WAS ADMITTED TO THE HOSPITAL, AND NEEDS SURGICAL INTERVENTION TO PREVENT INJURY OR PERMANENT DISABILITY. NO FURTHER INFORMATION PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
588348 NV GXL LINER NEUTRAL, 36MM ID, GROUP 2 CUPS PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, CEMENTED JDI EXACTECH, INC. 10885862207081

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Hospitalization