FDA Medical devices recall ·
Rifton Equipment, E-Pacer recall
- Recall number
- Z-1139-2026
- Date
- (initiated December 18, 2025)
- Company / brand
- Community Products, LLC
2032 Route 213, Rifton, NY, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 470 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
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.
Why was it recalled?
Potential for fraying on the body support strap.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
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, K66020170804AA, K66020170805AA, K66020170807AA, K66020170810AA, K66020170810AB, K66020170811AA, K66020170811AC, K66020170815AA, K66020170817AC, K66020170818AC, K66020170831AA, K66020170831AB, K66020170906AA, K66020170906AB, K66020170911AA, K66020170911AB, K66020170911AC, K66020170913AA, K66020170914AA, K66020170915AA, K66020170921AA, K66020170923AA, K66020170926AA, K66020170927AA, K66020170928AA, K66020171004AA, K66020171006AA, K66020171006AB, K66020171007AA, K66020171010AA, K66020171010AB, K66020171019AA, K66020171020AA, K66020171024AA, K66020171026AA, K66020171026AB, K66020171026AC, K66020171028AA, K66020171030AA, K66020171101AA, K66020171101AB, K66020171103AC, K66020171107AA, K66020171107AB, K66020171116AA, K66020171121AA, K66020171127AA, K66020171128AA, K66020171128AB, K66020171206AA, K66020171207AA, K66020171214AA, K66020171216AA, K66020171219AA, K66020171227AA, K66020171227AC, K66020180102AA, K66020180104AA, K66020180109AA, K66020180109AB, K66020180113AA, K66020180113AB, K66020180117AA, K66020180118AA, K66020180120AA, K66020180124AA, K66020180126AA, K66020180130AA, K66020180130AB, K66020180131AA, K66020180131AC, K66020
Distribution
Worldwide distribution - US Nationwide and the countries of UAE, Australia, Canada, EU, Israel, Hong Kong, Japan, Korea, New Zealand, Russia, Saudi Arabia, and UK.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1139-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.