# FDA recall Z-2530-2026

> **Zimmer, Inc.** · Class II · device recall initiated 2026-05-20.

## Product

Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040444

## Reason for recall

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

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2530-2026
- **Recalling firm:** Zimmer, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-20
- **Report date:** 2026-07-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2530-2026

## Citation

> MORVS. FDA recall Z-2530-2026. Retrieved 2026-10-16 from https://api.morvs.ai/recall/Z-2530-2026. Source: US FDA. Licensed CC0.

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