FDA Device recall Z-0165-2020
Rifton TRAM Low Base, SKU K320, 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 TRAM Low Base, SKU K320, 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-0165-2020 |
| 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 TRAM Low Base, SKU K320, 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: K32020130515AA K32020130603AA K32020130606AA K32020130607AA K32020130607AB K32020130610AA K320201306…ID Codes: K32020130515AA K32020130603AA K32020130606AA K32020130607AA K32020130607AB K32020130610AA K32020130612AA K32020130617AA K32020130617AB K32020130618AA K32020130709AA K32020130713AA K32020130713AB K32020130717AB K32020130730AA K32020130801AA K32020130802AA K32020130802AB K32020130805AA K32020130807AA K32020130808AA K32020130808AB K32020130812AA K32020130812AB K32020130812AC K32020130812AD K32020130813AA K32020130814AA K32020130820AA K32020130822AA K32020130823AA K32020130824AA K32020130827AA K32020130827AB K32020130828AA K32020130830AA K32020130830AB K32020130907AA K32020130909AA K32020130909AB K32020130909AC K32020130909AD K32020130909AE K32020130911AA K32020130912AA K32020130919AA K32020130920AA K32020130920AB K32020130924AA K32020131005AA K32020131007AA K32020131007AB K32020131008AA K32020131009AA K32020131017AB K32020131021AA K32020131022AB K32020131022AC K32020131022AD K32020131024AA K32020131025AA K3202013102 |
|---|
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-0165-2020%22
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