# FDA recall Z-1239-2018

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2018-01-24.

## Product

Coonrad/Morrey Elbow Implant System humeral assembly 4IN XSML, Item Number: 32-8105-027-04 (UDI: (01)0088902427 4006(17)220731(10)63694912)

## Reason for recall

One lot of humeral stem implants do not include the humeral bushing components.

## Distribution

Distributed in China and Taiwan.

## Key facts

- **Recall number:** Z-1239-2018
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-01-24
- **Report date:** 2018-04-04
- **Termination date:** 2019-04-09

- **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-1239-2018

## Citation

> AI Analytics. FDA recall Z-1239-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1239-2018. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*