Medical DeviceApr 10, 2024
SleepNet Mojo 2 Full Face AAV Non Vented Mask, All Sizes recall — FDA Z-1355-2024
Update to contraindications and warning language due to CPAP masks containing magnets.
Class IFDA: OngoingSleepNet Corporation
Recall history in this database
Classification mix: Class I: 7.
Medical DeviceApr 10, 2024
SleepNet iQ 2 Nasal Vented Mask recall — FDA Z-1356-2024
Update to contraindications and warning language due to CPAP masks containing magnets.
Class IFDA: OngoingSleepNet Corporation
Medical DeviceApr 10, 2024
SleepNet Mojo 2 Full Face Non Vented Mask, All Sizes recall — FDA Z-1354-2024
Update to contraindications and warning language due to CPAP masks containing magnets.
Class IFDA: OngoingSleepNet Corporation
Medical DeviceApr 10, 2024
SleepNet Mojo Non Vented Full Face Mask with Headgear, All Sizes recall — FDA Z-1352-2024
Update to contraindications and warning language due to CPAP masks containing magnets.
Class IFDA: OngoingSleepNet Corporation
Medical DeviceApr 10, 2024
SleepNet Mojo 2 Full Face Vented Mask, All Sizes recall — FDA Z-1353-2024
Update to contraindications and warning language due to CPAP masks containing magnets.
Class IFDA: OngoingSleepNet Corporation
Medical DeviceApr 10, 2024
SleepNet Phantom 2 Nasal Vented Mask recall — FDA Z-1357-2024
Update to contraindications and warning language due to CPAP masks containing magnets.
Class IFDA: OngoingSleepNet Corporation
Medical DeviceApr 10, 2024
SleepNet Mojo Full Face with Headgear, All Sizes recall — FDA Z-1351-2024
Update to contraindications and warning language due to CPAP masks containing magnets.
Class IFDA: OngoingSleepNet Corporation
Understanding this recall history
This page summarizes recall records in which the official source identifies SleepNet Corporation as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.