RegWardenFDA facility compliance records
Facility

JK PRODUCTS & SERVICES, INC.

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

Activity by year

FDA actions on record by yearEarlier: 1 recalls; 2012: 1 recalls; 2014: 1 recalls; 2017: 1 inspections1Earlier’08’09’10’111’12’131’14’15’161’17’18’19’20’21’22’23’24’25’26
  • Recalls (3)
  • Inspections (1)

Devices registered here (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…

FDA inspections (1)

  • NAI2017-02-24
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices; Radiation Control and Health Safety Act

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “JK PRODUCTS & SERVICES, INC. (FEI 2311923) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2311923-jk-products-services-inc/

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