Community Products, LLC recalls Rifton Equipment

Potential for fraying on the body support strap.

Community Products notified consignees via email on about 12/18/2025. Consignees were instructed to notify all customers, if further distributed, of the recall, inspect all affected devices for visible fraying, and cease use if any is observed. Consignees were requested to provide contact information for the individual responsible for performing the replacement. If devices were further distributed, consignees were advised to manage all customer outreach, inspection and replacement. The other option was to provide Community Products with customer contact information, and Rifton will manage the process. Lastly, consignees were requested to confirm receipt of the notification.

• FDA enforcement recordOfficial FDA database entry for Z-1139-2026
• FDA device classification · FSAOfficial FDA classification for this device type
• CFR regulation · 21 CFR 880.5510The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Community Products, LLCSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.