# FDA device recall: Off-Axis Comprehensive Shoulder System Small, Augment, Off-Axis, Reamer Guide, Model/Catalog Number: 110040240

> recall · VERIFIED · 2026-05-20

Firm: Zimmer, Inc. · Class II · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.

- Company: Zimmer, Inc.
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.