# FDA recall Z-1222-2023

> **OMM Imports, Inc. dba Zero Gravity** · Class II · device recall initiated 2022-09-01.

## Product

Recreo Hair Growth Laser Comb

## Reason for recall

The firm distributed the laser products without affixing the warning, aperture, certification, and identification labels. In addition, the firm failed to provide safety information, reproductions and locations of the labels, and a warning statement in the user manual.

## Distribution

Worldwide and Nationwide including DC and Puerto Rico

## Key facts

- **Recall number:** Z-1222-2023
- **Recalling firm:** OMM Imports, Inc. dba Zero Gravity
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-09-01
- **Report date:** 2023-03-22

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1222-2023

## Citation

> AI Analytics. FDA recall Z-1222-2023. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1222-2023. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
