# FDA recall Z-1098-2023

> **Zimmer, Inc.** · Class II · device recall initiated 2022-12-07.

## Product

Identity Shoulder System Resection Planer 35mm Resection Planer

## Reason for recall

Two planers were found to be unusable during sawbones shoulder training.

## Distribution

US Nationwide distribution in the states of AR, CA, IL, MI, NJ, NY, OK, PA, TX, and WA.

## Key facts

- **Recall number:** Z-1098-2023
- **Recalling firm:** Zimmer, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-12-07
- **Report date:** 2023-02-15

- **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-1098-2023

## Citation

> AI Analytics. FDA recall Z-1098-2023. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1098-2023. Source: US FDA. Licensed CC0.

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