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Jk Products & Services, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 2311923

Devices
0
Registrations
FDA
FDA recalls
3

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
2311923
Address
1823 Grant Ave Ste A, JONESBORO, AR, 72401

FDA recalls3

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

  • 2014

    • 25 Jul 2014 Z-2635-2014 Class II Terminated The integrity of the wires inside main electrical chord become compromised from excessive flexing (during the door open/close process). Distribution: Nationwide Distribution. Submission number: K932483

  • 2012

    • 7 May 2012 Z-2183-2012 Class II Terminated The Beauty Angel was marketed without a 510k. Distribution: Worldwide Distribution - USA (nationwide) and Canada

  • 2005

    • 8 Jul 2005 Z-2334-2012 Class II Terminated 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 point in the cord. Distribution: Worldwide Distribution - USA (nationwide) and Canada

This is an FDA establishment record without devices in deviCERTS.