ProductGuru Recalls

Official recall record

Community Products, Llc Dba Rifton Equipment

Health Canada — Medical Devices · 2025-12-18 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-12-18
Last updated (per notice)
2025-12-17
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Rifton initiated recalls for TRAM and E-Pacer units due to an unrelated buckle spring failure, which led to replacing the full body support strap assembly. for that recall, rifton ordered a large batch of aluminum stampings (DA53). Because of the unusually large order, the supplier used a different manufacturing process, resulting in some stampings having sharper strap openings. over time, these sharp edges can abrade and fray the straps, and if not addressed, may cause the strap to fail, creating a fall risk for the user.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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