The Recall Desk

Manufacturer

JK Products & Services, Inc

3 recalls in our database name JK Products & Services, Inc as the manufacturing or recalling firm.

What the numbers show

Total
3
Critical
0
Severe
0
Most recent
2014-09-24

Of the 3 recalls from JK Products & Services, Inc we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–3 of 3

  • HighFDA (Devices)·Z-2635-2014·2014-09-24

    JK Products Recalls Sun Dash Radius 252 Tanning Beds Due to Electrical Hazard

    JK Products & Services is recalling 1,948 Sun Dash Radius 252 tanning beds because excessive flexing of the main electrical cord can compromise wire integrity.

    Product
    SUN DASH RADIUS 252 PN 8000809705. The device is intended to be used for the tanning of human skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2334-2012·2012-09-19

    JK Products Recalls Sun|Dash Radius 252 Tanning Systems Due to Wiring Short

    JK Products & Services is recalling 1,948 Sun|Dash Radius 252 tanning systems because a door cord failure can cause a short in the wiring.

    Product
    SUN|DASH RADIUS 252 tanning system; 52 lamps, Ultraviolet Radiation. The device is intended to be used for tanning of the human skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2183-2012·2012-08-22

    Beauty Angel Device Recalled for Lack of FDA Clearance

    JK Products & Services is recalling Beauty Angel devices because they were marketed without the required FDA 510(k) clearance.

    Product
    BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human use.
    Category
    Medical Device
    Distribution
    Distributed nationwide