# FDA recall Z-0803-2018

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2017-09-07.

## Product

The 2nd Assist Knee Positioner

## Reason for recall

Zimmer Biomet is conducting a medical device recall for the 2nd Assistant Knee Positioner due to the potential for the sterile packaging barrier to be breached during distribution.

## Distribution

Nationally

## Key facts

- **Recall number:** Z-0803-2018
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-09-07
- **Report date:** 2018-03-07
- **Termination date:** 2018-08-23

- **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-0803-2018

## Citation

> AI Analytics. FDA recall Z-0803-2018. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/Z-0803-2018. Source: US FDA. Licensed CC0.

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