Atlas FDA

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

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