medical MODERATE Updated 2026-07-01

Zimmer, Inc. recalls Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Gui

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Recalled Product

Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040476

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Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot Code: Model No. 110040476 ; UDI-DI (01)00889024682047(17)350531(10)097492 ; Lot Number 097492

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

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