# FDA recall Z-1939-2020

> **Remel Inc.** · Class II · device recall initiated 2019-01-04.

## Product

SWIN 2017 database, Model YSW4000

## Reason for recall

Potential for out of range microbial results

## Distribution

...

## Key facts

- **Recall number:** Z-1939-2020
- **Recalling firm:** Remel Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-01-04
- **Report date:** 2020-05-20
- **Termination date:** 2020-08-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Oakwood Village, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1939-2020

## Citation

> AI Analytics. FDA recall Z-1939-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1939-2020. Source: US FDA. Licensed CC0.

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