Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1137-2026 — 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.

U.S. FDA — Device Enforcement · United States · 2025-12-18 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1137-2026
Date of alert: 2025-12-18
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Community Products, LLC
Product category: device
Product type: Devices

Reported risk: Potential for fraying on the body support strap.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-1137-2026 — 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.

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