Class II — JK Products & Services, Inc
| Recalling firm | JK Products & Services |
|---|---|
| Registered facility | JK PRODUCTS & SERVICES, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process). |
| Product | SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin. |
| Quantity | 1948 units |
| Distribution | Nationwide Distribution. |
| Initiated | 2014-07-25 |
| Classified | 2014-09-12 |
| Terminated | 2017-01-13 |
| Recall number | Z-2635-2014 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — JK Products & Services, Inc (Z-2635-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/69038/
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