inforMED
InjuryPAO

DJO SURGICAL

Received Jun 29, 2026 · Event occurred Jun 11, 2026

Report 1644408-2026-01255 · MDR key 25650348

Device

Generic name

Altivate Anatomic, All-poly Pegged Glenoid, Size 38, E-plus

Catalog number

521-07-238

Lot number

890U1102

Product problems

  • Patient Device Interaction Problem

Patient

54 YR · Female

  • Unspecified Infection
  • Joint Laxity

Narrative

Description of Event or Problem

REVISION SURGERY DUE TO THE PATIENT HAD LOOSENING OF THE GLENOID IMPLANT AND SUSPECTED INFECTION.

Additional Manufacturer Narrative

THE AGENT REPORTED THE PATIENT HAD LOOSENING OF THE GLENOID IMPLANT AND SUSPECTED INFECTION. FEMALE 54. COMPLAINT HAS BEEN EVALUATED AND IS SIMILAR TO REPORT NUMBER 1644408-2022-01081; 521-07-250, S810 - DEVICE LOOSENING, S808 - INFECTION, REVISION SURGERY. IF ADDITIONAL INFORMATION REGARDING THE REPORTED EVENT IS SUBMITTED AT A FUTURE DATE, THIS INVESTIGATION WILL BE RE-EVALUATED.