Global Recall Issued for Sleepnet CPAP and BiPAP Masks Containing Magnets
In March 2024, a worldwide recall was initiated for all Sleepnet CPAP and BiPAP masks containing magnets, including the Mojo, Mojo 2, iQ 2, and Phantom 2 masks, due to risks of interference with other medical implants. These magnets could potentially cause the implants to malfunction or move, posing severe risks to individuals with certain medical implants.
The recall was confirmed by the FDA following Sleepnet’s announcement at the beginning of March after post-market surveillance identified the issue. While there have been no reported injuries or deaths associated with the recalled masks, the FDA has classified it as a Class I recall, indicating a high risk of serious injuries or death.
