Class I — SleepNet Corporation
| Recalling firm | SLEEPNET CORPORATION |
|---|---|
| Registered facility | SLEEPNET CORPORATION (the firm's only registered facility) |
| Classification | Class I |
| Status | Ongoing |
| Reason | Update to contraindications and warning language due to CPAP masks containing magnets. |
| Product | Mojo Non Vented Full Face Mask with Headgear, All Sizes |
| Quantity | 11,874 units |
| 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, … |
| Initiated | 2024-03-01 |
| Classified | 2024-04-01 |
| Recall number | Z-1352-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class I recall — SleepNet Corporation (Z-1352-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94169/
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