FDA Device recall Z-0166-2020
Rifton E-Pacer, SKU K660, powered lift device
- FDA Device
- Class II
- terminated
- Published 2019-10-30
On 2019-10-30 the FDA classified a Class II recall of Rifton E-Pacer, SKU K660, powered lift device by Community Products, citing A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0166-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-03-21 |
| Published | 2019-10-30 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Community Products |
| Distribution | US |
Product
Rifton E-Pacer, SKU K660, powered lift device
Reason
A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
Identifiers
| code_info | ID Codes: K66020170425AA K66020170612AA K66020170621AA K66020170622AA K66020170626AA K66020170626AB K66020170626…ID Codes: K66020170425AA K66020170612AA K66020170621AA K66020170622AA K66020170626AA K66020170626AB K66020170626AC K66020170627AC K66020170627AD K66020170628AA K66020170629AA K66020170703AA K66020170705AA K66020170711AA K66020170712AA K66020170712AC K66020170713AB K66020170713AC K66020170716AA K66020170717AA K66020170717AB K66020170804AA K66020170805AA K66020170807AA K66020170810AA K66020170810AB K66020170811AA K66020170811AC K66020170815AA K66020170817AB 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 K66020171101A |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0166-2020%22
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