Mojo Non Vented Full Face Mask with Headgear, All Sizes

Recall Insight

This FDA Devices action (record #Z-1352-2024) was formally reported on April 10, 2024, with the manufacturer initiating the action on March 1, 2024. It is classified under Critical severity (Class I), with a current status of Ongoing. SleepNet Corporation is listed as the recalling firm, operating out of Hampton, NH. Federal records indicate 11,874 units units are affected.

The documented reason for this recall is: Update to contraindications and warning language due to CPAP masks containing magnets. Distribution data in the federal record shows the product reached: Worldwide distribution - US Nationwide and the countries of AUSTRIA, BAHRAIN, BRAZIL, COLOMBIA, COSTA RICA, ECUADOR, EL SALVADOR, FINLAND, FRANCE, GERMANY, GREAT BRITAIN, GREECE, INDIA, IRAQ, IRELAND, ISRAEL, ISREAL, IT…. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC and NHTSA going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Devices. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 2 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.