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Zimmer, Inc. recalls Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241
Recalled July 1, 2026 · FDA recall Z-2528-2026 · Zimmer
Hazard
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. · FDA Class II
Units
435 units
Sold at
US Nationwide distribution.
Description
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
Product
Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide Model/Catalog Number: 110040241
Manufacturer(s)
Zimmer, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →