SleepNet recalls all iQ 2 Nasal Vented Masks due to updated magnet safety warnings. This change addresses potential risks from CPAP masks containing magnets.
Update to contraindications and warning language due to CPAP masks containing magnets.
SleepNet is recalling all iQ 2 Nasal Vented Masks because they contain magnets that could pose safety risks. This update is part of improved contraindications and warning language for CPAP masks.
CPAP masks with magnets can cause issues for people with certain medical conditions, such as pacemakers or other implanted devices. The updated warnings address potential risks from these magnets.
People using SleepNet iQ 2 Nasal Vented Masks are affected. Those with medical conditions that could be impacted by magnets are at higher risk.
The recalled product is the SleepNet iQ 2 Nasal Vented Mask. All units with UDI-DI and all lot numbers are included in this recall.
Look for the product name and lot numbers on the mask packaging.
The recall updates contraindications and warning language due to magnets in CPAP masks.
No specific stop-use instruction is provided; the recall focuses on updated safety warnings.
All SleepNet iQ 2 Nasal Vented Masks with UDI-DI and all lot numbers are included in this recall.
We’ve drafted a message you can send SleepNet to request your refund or repair — edit it as you like.
Subject: Recall Z-1356-2024 — SleepNet SleepNet Hello, I own a SleepNet that is covered by recall Z-1356-2024 from SleepNet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
