FDAClass IISeptember 24, 2014

SUN DASH RADIUS 252 PN 8000809705. The device is recall

SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.

Why was SUN DASH RADIUS 252 PN 8000809705. The device is recalled?

The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process).

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

PN 8000809705; Serial numbers 248-1298

Product
SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.
Recalling firm
JK Products & Services, Inc
Quantity
1948 units
Distribution
Nationwide Distribution.
Recall date
September 24, 2014
Classification
Class II
Status
Terminated
Agency
FDA (device)
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