FDA
Food and Drug Administration · Recall Z-2530-2026 · May 20, 2026Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040444
Zimmer, Inc.
The hazard
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040444
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model Lot Code: 110040444Model UDI-DI (01)00889024681903(17)350531(10)097487Model Lot Number 097487UPC 00889024681903Would you have heard about this one?
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Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.