Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transfe
Pending LLM rewrite. Source: FDA_DEVICE Z-1137-2026.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
Potential for fraying on the body support strap.
The recalled product
- Product
- Rifton Equipment, TRAM. Model/Catalog Number: K310. 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.
- Manufacturer
- Community Products, LLC
- Category
- Medical Device — Devices
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 (20)
- Model/Catalog Number: K310. ID Codes: K31020120704AA
- K31020120706AA
- K31020120707AC
- K31020120707AD
- K31020120707AE
- K31020120707AG
- K31020120709AA
- K31020120709AB
- K31020120709AD
- K31020120709AE
- K31020120710AB
- K31020120710AE
- K31020120711AB
- K31020120712AA
- K31020120713AB
- K31020120713AC
- K31020120713AD
- K31020120713AF
- K31020120718AA
- K31020120718AB
Distribution
Distributed nationwide across the United States.
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