# FDA recall Z-0720-2022

> **Sunstar Americas, Inc.** · Class II · device recall initiated 2022-01-14.

## Product

BUTLER Clear Dip, 12 bottles/case

## Reason for recall

Product lacks premarket clearance.

## Distribution

United States Nationwide distribution.

## Key facts

- **Recall number:** Z-0720-2022
- **Recalling firm:** Sunstar Americas, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-01-14
- **Report date:** 2022-03-09
- **Termination date:** 2023-08-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Schaumburg, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0720-2022

## Citation

> AI Analytics. FDA recall Z-0720-2022. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-0720-2022. Source: US FDA. Licensed CC0.

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