SleepNet recalls Mojo 2 Full Face Vented Masks due to magnet safety concerns. Update to contraindications and warning language for CPAP masks with magnets.
Update to contraindications and warning language due to CPAP masks containing magnets.
SleepNet is recalling all Mojo 2 Full Face Vented Masks because they contain magnets that could pose safety risks. This update addresses potential contraindications and warning language for CPAP users.
The masks contain magnets that could pose risks for people with medical implants or conditions sensitive to magnets. This update addresses potential contraindications and warning language for CPAP users.
CPAP users with the Mojo 2 Full Face Vented Mask are affected. Those with medical conditions that could be impacted by magnets are at higher risk.
Check for the Mojo 2 Full Face Vented Mask with all sizes. The recall includes all units with UDI-DI and all lot numbers.
Check the product label for the model name and lot number to confirm if it's recalled.
The recall updates contraindications and warning language due to magnets in CPAP masks.
No specific stop-use instruction is given; the recall focuses on updating safety information.
Check the product label for the model name and lot number to confirm if it's recalled.
We’ve drafted a message you can send SleepNet to request your refund or repair — edit it as you like.
Subject: Recall Z-1353-2024 — SleepNet SleepNet Hello, I own a SleepNet that is covered by recall Z-1353-2024 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.
