[pending] 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.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Pending LLM scoring against the rubric.
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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