Rifton E-Pacer — Class II medical device recall Z-0166-2020
Terminated recall by Community Products, LLC, reported 2019-10-30, distributed nationwide. A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptibl
| Recall number | Z-0166-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Community Products, LLC, Rifton, NY, United States |
| Recall initiated | 2019-03-21 |
| Classified | 2019-10-22 |
| Reported by FDA | 2019-10-30 |
| Terminated | 2020-06-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, CA, CO, DE, DK, IE, IL, IT, JP, KR, NZ, RU, SG, TW |
| Quantity | 167 |
Product
Rifton E-Pacer, SKU K660, powered lift device
Reason for recall
A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
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-0166-2020. 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.