FDAFDA · Food and drugs·Recall number Z-2530-2026
Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040444
Published July 1, 2026 · Recall initiated: May 20, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.
What to do
Voluntary: Firm initiated
Recall details
- Manufacturer
- Zimmer, Inc.
- Distributor
- US Nationwide distribution.
- Lot
- Lot Code: 110040444 ; UDI-DI (01)00889024681903(17)350531(10)097487 ; Lot Number 097487
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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