RegWardenFDA facility compliance records
Company

JK Products & Services

3 recall(s) on record — most severe on record: Class II.

Recalls by year

FDA actions on record by yearEarlier: 1 recalls; 2012: 1 recalls; 2014: 1 recalls1Earlier’08’09’10’111’12’131’14’15’16’17’18’19’20’21’22’23’24’25’26
  • Recalls (3)

Registered facilities (1)

Recalls & enforcement

  • Class IITerminated2014-07-25
    The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process).
  • Class IITerminated2012-05-07
    The Beauty Angel was marketed without a 510k.
  • Class IITerminated2005-07-08
    The firm has tracked a systematic failure in the door cord on the Sun|Dash Radius 252 product line. In some instances when the door cord is installed with little or no slack outside the upper decor piece, the cord has been known to fail causing a short in the wiring at the pivot…

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.

Cite this record

RegWarden. “JK Products & Services — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-2311923-jk-products-services/

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