RegWardenFDA facility compliance records
Company

Quality Electrodynamics

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

Recalls by year

FDA actions on record by year2012: 1 recalls; 2019: 1 recalls1’12’13’14’15’16’17’181’19’20’21’22’23’24’25’26
  • Recalls (2)

Registered facilities (1)

Recalls & enforcement

  • Class IITerminated2019-08-20
    Unintended ferrous material may be present within the pushbutton assembly of Siemens Knee and Siemens Extremity Coils.
  • Class IITerminated2012-07-27
    On July 27, 2012, it was reported to the firm that the Siemens 3T 15ch Knee Coil was not functional because the coil identification code for the device was incorrect.

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. “Quality Electrodynamics — 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-10023379-quality-electrodynamics/

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