Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device wit
Pending LLM rewrite. Source: FDA_DEVICE Z-1139-2026.
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, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device with power height adjustment that facilitates the sit-to-stand motion.
- 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: K660. ID Codes: K66020170425AA
- K66020170612AA
- K66020170621AA
- K66020170622AA
- K66020170626AA
- K66020170626AB
- K66020170626AC
- K66020170627AC
- K66020170627AD
- K66020170628AA
- K66020170629AA
- K66020170703AA
- K66020170705AA
- K66020170711AA
- K66020170712AA
- K66020170712AC
- K66020170713AB
- K66020170716AA
- K66020170717AA
- K66020170717AB
Distribution
Distributed nationwide across the United States.
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