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Terminated

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

FDA Recall Z-2635-2014 · Posted 2014-09-12

Recalling FirmJK Products & Services, Inc
Recall StatusTerminated
Product CodeLEJ
Date Initiated2014-07-25
Date Terminated2017-01-13
Product Quantity1948 units

Reason for Recall

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

Firm Action

The owners of the affected device will be notified via certified letter. After the recalling firm confirms ownership, a technician will be dispatched to install a door clamp and door stop, and inspect the condition of the main electrical chord.

Root Cause

Device Design

Distribution Pattern

Nationwide Distribution.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K932483SUNDASHSun Ind., Inc. · 1994-02-22

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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