Powered lift transfer devices recalled over potential fraying on support straps
Community Products is recalling 1,096 units of the Rifton Low Base TRAM over potential fraying on the body support strap.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: Scored 2 because the record cites potential fraying on a component with no stated consequence or reported harm.
Plain-English summary
Rifton Equipment Low Base TRAM, model/catalog number K320, is being recalled by Community Products, LLC. The record describes the product as follows: The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training, and the record states the low base variant includes smaller casters.
The reason given in the enforcement record is a potential for fraying on the body support strap.
The record lists 1,096 units under model K320, with ID codes recorded in the enforcement record. Distribution was worldwide, covering the United States nationwide and the UAE, Australia, Canada, the EU, Israel, Hong Kong, Japan and other countries listed in the record. The FDA has classified the action as Class II.
The record names no consequence and reports no injuries. Facilities and users should follow the firm's instructions, including any guidance on inspecting the strap.
The recalled product
- Product
- MEAL SIMPLE RED LENTIL DAL SOUP NET WT. 16 OZ (1 LB) 454g UPC 1 97870 07333 0 MADE WITH PRIDE AND CARE FOR H-E-B-, SAN ANTONIO, TEXAS 78204
- Manufacturer
- Bakkavor
- Category
- Medical Device — Patient lift
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot: 882428 Best By Date 1/11/2026
Distribution
Distributed in 1 state:
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