# FDA recall Z-1000-2020

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2019-12-12.

## Product

Coonrad/Morrey Total Elbow Humeral Assembly, Extra Small, 4-inch Length. Model No. 32-8105-027-04. UDI (01)00889024274006 (17)241031(10)64481139    The device is a Humeral component; elbow joint metal/polymer constrained cemented prosthesis.

## Reason for recall

The lot contained two outer pins instead of one outer and one inner pin.

## Distribution

Distributed to accounts in California and Ohio.

## Key facts

- **Recall number:** Z-1000-2020
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-12-12
- **Report date:** 2020-02-12
- **Termination date:** 2021-01-13

- **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-1000-2020

## Citation

> AI Analytics. FDA recall Z-1000-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1000-2020. Source: US FDA. Licensed CC0.

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