FDA Device recall Z-1356-2024
iQ 2 Nasal Vented Mask
- FDA Device
- Class I
- ongoing
- Published 2024-04-10
On 2024-04-10 the FDA classified a Class I recall of iQ 2 Nasal Vented Mask 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-1356-2024 |
| 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
iQ 2 Nasal Vented Mask
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-1356-2024%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.