RegWardenFDA facility compliance records
Company

IDS CO, LTD

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

Recalls by year

FDA actions on record by year2012: 1 recalls; 2024: 1 recalls1’12’13’14’15’16’17’18’19’20’21’22’231’24’25’26
  • Recalls (2)

Registered facilities (2)

Recalls & enforcement

  • Class IIOngoing2024-10-16
    The Smaxel Fractional CO2 Laser does not include a Certification label, and adequate instructions for safe operation of the device.
  • Class IITerminated2012-11-07
    Immunodiagnostic Systems is recalling the 25-Hydroxy Vitamin D EIA, AC-57F1 because the QC report was found to have an erroneous calibrator value assigned. The value of 24.4 ng/mL for calibrator 4 was stated on the QC report, however the correct value should have read 28.4 ng/mL…

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. “IDS CO, LTD — 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-10049986-ids-co-ltd/

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