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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:172029

Rifton E-Pacer, SKU K660, powered lift device

Official recall number

Z-0166-2020

Evidence summary

Product code
FSA
Recall status
Terminated
Event initiated
March 21, 2019
Root cause
Nonconforming Material/Component
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-0166-2020

Field note

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