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On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.

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  1. Radiation Safety

Report a Problem

Manufacturers of electronic products must report to FDA all accidental radiation occurrences arising from the manufacturing, testing, or use of any product introduced or intended to be introduced into commerce. For more information about reporting problems or hazards, see Reports and Recordkeeping.

Manufacturers and anyone in the general public may use the following fillable form to submit a report on any radiation incident or potentially hazardous event: Accidental Radiation Occurrence Report

Health professionals and consumers can also report problems with medical products including serious reactions, product quality problems and product use errors. For more information about submitting a report, see MedWatch: The FDA Safety Information and Adverse Event Reporting Program.



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