# FDA recall Z-0319-2018

> **ProSun International, LLC** · Class II · device recall initiated 2017-12-02.

## Product

Sundream 12 V tanning bed

## Reason for recall

The 30 minute maximum tanning time has been reduced to 20 minutes.

## Distribution

Distributed domestically to AK, AL, AZ, CA, CT, FL, GA, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NV, NY, OH, OK, PA, SC, TN, TX, UT, WA, WI

## Key facts

- **Recall number:** Z-0319-2018
- **Recalling firm:** ProSun International, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-02
- **Report date:** 2018-01-17
- **Termination date:** 2026-02-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Petersburg, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0319-2018

## Citation

> AI Analytics. FDA recall Z-0319-2018. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0319-2018. Source: US FDA. Licensed CC0.

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