FDA Device recall Z-0164-2020
Rifton TRAM Standard Base, SKU K310, 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 Standard Base, SKU K310, 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-0164-2020 |
| 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 Standard Base, SKU K310, 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: K31020120704AA K31020120706AA K31020120707AC K31020120707AD K31020120707AE K31020120707AG K310201207…ID Codes: K31020120704AA K31020120706AA K31020120707AC K31020120707AD K31020120707AE K31020120707AG K31020120709AA K31020120709AB K31020120709AD K31020120709AE K31020120710AA K31020120710AB K31020120710AE K31020120711AA K31020120711AB K31020120712AA K31020120712AB K31020120713AB K31020120713AC K31020120713AD K31020120713AE K31020120713AF K31020120718AA K31020120718AB K31020120718AC K31020120719AC K31020120720AA K31020120727AA K31020120727AB K31020120801AA K31020120804AB K31020120804AC K31020120804AD K31020120804AH K31020120804AI K31020120806AA K31020120806AB K31020120806AC K31020120806AD K31020120806AE K31020120806AG K31020120806AH K31020120806AI K31020120806AK K31020120806AL K31020120806AM K31020120806AN K31020120806AO K31020120807AA K31020120807AB K31020120807AC K31020120807AD K31020120807AE K31020120807AF K31020120809AD K31020120809AE K31020120810AC K31020120813AB K31020120813AE K31020120814AA K31020120814AB K3102012081 |
|---|
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-0164-2020%22
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