RegWardenFDA facility compliance records
Company

Mirion Technologies, Inc.

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

Recalls by year

FDA actions on record by year2023: 1 recalls; 2024: 1 recalls; 2026: 1 recalls2017201820192020202120221202312024202512026
  • Recalls (3)

Registered facilities (2)

Recalls & enforcement

  • Class IIOngoing2026-07-20
    Potential for failure of the tension bolt which would allow the spring arm to unexpectedly fall to its lowest position, which is approximately 25 inches (63.5 cm) from the ground.
  • Class IIOngoing2024-04-22
    Complaints of unexpected detachment of the collimator have been reported.
  • Class IIOngoing2023-11-27
    Spring arm failure with Captus 4000e Thyroid Uptake Systems, can cause the collimator to fall downward to its lowest point of travel, causing potential injury with a patient or operator

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. “Mirion Technologies, Inc. — 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-10043529-mirion-technologies-inc/

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