Consumer Alerts Tracker
openFDA Medical device

Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241

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

Official details

Category
Medical device recall
Status
Ongoing
Classification
Class II
Company or vendor
Zimmer, Inc.
Affected product
US Nationwide distribution.
Risk or reason
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Remedy or action
Lot Code: Model No. 110040241 ; UDI-DI (01)00889024681941(17)350602(10)099463 ; Lot Number 099463 Model No. 110040241 ; UDI-DI (01)00889024681941(17)350531(10)099464 ; Lot Number 099464 Model No. 110040241 ; UDI-DI (01)00889024681941(17)350812(10)099465 ; Lot Number 099465 Model No. 110040241 ; UDI-DI (01)00889024681941(17)350707(10)099467 ; Lot Number 099467
Official ID
Z-2528-2026