Medical Device

Off-Axis Comprehensive Shoulder System, Large, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040242

Recall date: 2026-07-01 · Source: FDA_DEVICE

Brand / Firm

Product

Reason for recall

Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.

Units affected

429 units

Description

Off-Axis Comprehensive Shoulder System, Large, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040242