RegWardenFDA facility compliance records
Company

Paragonix Technologies

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

Recalls by year

FDA actions on record by year2026: 1 recalls20172018201920202021202220232024202512026
  • Recalls (1)

Registered facilities (1)

Recalls & enforcement

  • Class IIOngoing2026-07-20
    Due to a firmware defect, the portable organ transfer device datalogger may lose its configuration, resulting in a blank screen and loss of displayed preservation parameters.

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. “Paragonix Technologies — 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-10057453-paragonix-technologies/

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