Rifton Equipment, Low Base TRAM. Model/Catalog Number: K320. The TRAM is a powered lift device for transferring clients
FDA device recall Z-1138-2026 · posted 2026-01-22 · Open, Classified
Recall details
- Recalling firm
- Community Products, LLC
- Reason for recall
- Potential for fraying on the body support strap.
- Action taken
- 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.
- Root cause
- Process change control
- Status
- Open, Classified
- Product code
- FSA
- Quantity affected
- 1,096 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of UAE, Australia, Canada, EU, Israel, Hong Kong, Japan, Korea, New Zealand, Russia, Saudi Arabia, and UK.
- Date initiated
- 2025-12-18
- Date posted
- 2026-01-22
- Location
- Rifton, NY
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.