# FDA recall Z-1352-2024

> **SleepNet Corporation** · Class I · device recall initiated 2024-03-01.

## Product

Mojo Non Vented Full Face Mask with Headgear, All Sizes

## Reason for recall

Update to contraindications and warning language due to CPAP masks containing magnets.

## Distribution

Worldwide distribution - US Nationwide and the countries of AUSTRIA, BAHRAIN, BRAZIL, COLOMBIA, COSTA RICA, ECUADOR, EL SALVADOR, FINLAND, FRANCE, GERMANY, GREAT BRITAIN, GREECE, INDIA, IRAQ, IRELAND, ISRAEL, ISREAL, ITALY, JAPAN, JORDAN, KUWAIT, LEBANON, MALAYSIA, MEXICO, MOROCCO, NORWAY, POLAND, QATAR, ROMANIA, RUSSIA, SAUDI ARABIA, SLOVAKIA, SOUTH AFRICA, SOUTH KOREA, SPAIN, SULTANATE OF OMAN, SWEDEN, SWITZERLAND, THE NETHERLANDS, TURKEY, UNITED ARAB EMIRATES, UNITED KINGDOM, URUGUAY, VIETNAM, YEMEN.

## Key facts

- **Recall number:** Z-1352-2024
- **Recalling firm:** SleepNet Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-01
- **Report date:** 2024-04-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Hampton, NH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1352-2024

## Citation

> AI Analytics. FDA recall Z-1352-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1352-2024. Source: US FDA. Licensed CC0.

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