Food, drugs, devices › JK Products & Services, Inc
Device recall: SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.
FDA enforcement event 69038 is a device recall by JK Products & Services, Inc of Jonesboro, AR, initiated 25 Jul 2014 and classified Class II, with 1 product record.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 91% of the 1,176 device enforcement events initiated in 2014 carry the same class.
Status: Terminated, terminated 13 Jan 2017. Initiation: voluntary: firm initiated. JK Products & Services, Inc has 3 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
JK Products & Services, Inc, Jonesboro, AR.
Reason for recall
"The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process)."
Distribution
"Nationwide Distribution."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-2635-2014 | SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin. | 1948 units | Class II | Terminated | 24 Sep 2014 |
Context
Other enforcement events for JK Products & Services, Inc
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 7 May 2012 | BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human use. | Device | Class II | 1 |
| 8 Jul 2005 | SUN|DASH RADIUS 252 tanning system; 52 lamps, Ultraviolet Radiation. The device is intended to be used for tanning of th | Device | Class II | 1 |
All 3 events for JK Products & Services, Inc
Questions and answers
Why was this device recalled?
FDA's record gives the reason for recall as: "The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process)."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "Nationwide Distribution."
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 13 Jan 2017. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.