# FDA recall Z-0871-2020

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2019-12-19.

## Product

ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp  Mode Number: 110032332    Product Usage:  The device is a general orthopedic manual surgical instrument

## Reason for recall

Potential issue associated with the instrument -end of the shaft could fail to effectively mate with the broach

## Distribution

US Nationwide and Foreign: countries of Canada, CHINA, NETHERLANDS

## Key facts

- **Recall number:** Z-0871-2020
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-12-19
- **Report date:** 2020-02-05
- **Termination date:** 2020-08-11

- **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-0871-2020

## Citation

> AI Analytics. FDA recall Z-0871-2020. Retrieved 2026-06-22 from https://api.ai-analytics.org/recall/Z-0871-2020. Source: US FDA. Licensed CC0.

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