# FDA recall Z-1500-2022

> **Craftmatic Industries, Inc.** · Class II · device recall initiated 2017-03-24.

## Product

Legacy Base for Dual Bed Configurations

## Reason for recall

A potential for dual-configured beds to separate or slip away from one another.

## Distribution

US Nationwide distribution - product was not distributed outside of the United States

## Key facts

- **Recall number:** Z-1500-2022
- **Recalling firm:** Craftmatic Industries, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2017-03-24
- **Report date:** 2022-08-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Pompano Beach, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1500-2022

## Citation

> AI Analytics. FDA recall Z-1500-2022. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1500-2022. Source: US FDA. Licensed CC0.

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