Rifton Equipment — Class II medical device recall Z-1139-2026
Ongoing recall by Community Products, LLC, reported 2026-01-28, distributed nationwide. Potential for fraying on the body support strap.
| Recall number | Z-1139-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Community Products, LLC, Rifton, NY, United States |
| Recall initiated | 2025-12-18 |
| Classified | 2026-01-22 |
| Reported by FDA | 2026-01-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, CA, GB, HK, IL, JP, KR, NZ, RU, SA |
| Quantity | 470 units |
| Model numbers | K660, K66020170425AA, K66020170612AA, K66020170621AA, K66020170622AA, K66020170626AA, K66020170626AB, K66020170626AC, K66020170627AC, K66020170627AD, K66020170628AA, K66020170629AA, K66020170703AA, K66020170705AA, K66020170711AA, K66020170712AA, K66020170712AB, K66020170712AC, K66020170713AA, K66020170713AB, K66020170713AD, K66020170713AE, K66020170716AA, K66020170717AA, K66020170717AB and 454 more |
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.
Reason for recall
Potential for fraying on the body support strap.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1139-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.