FDA Device recall Z-1352-2024
Mojo Non Vented Full Face Mask with Headgear, All Sizes
- FDA Device
- Class I
- ongoing
- Published 2024-04-10
On 2024-04-10 the FDA classified a Class I recall of Mojo Non Vented Full Face Mask with Headgear, All Sizes by Sleepnet, citing update to contraindications and warning language due to CPAP masks containing magnets.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1352-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2024-03-01 |
| Published | 2024-04-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Sleepnet |
| Distribution | US |
Product
Mojo Non Vented Full Face Mask with Headgear, All Sizes
Reason
Update to contraindications and warning language due to CPAP masks containing magnets.
Identifiers
| code_info | All UDI-DI; All Lot Numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1352-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.