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FDA Warning Regarding Breast Implants:

VIEW FDA STATEMENT

Below Are The Instructions To Submit An "Adverse Event Report to FDA"

Here is the information for Submitting Adverse Event Reports to FDA. Please Use one of the methods below to submit voluntary adverse event reports to the FDA:

1. Report online at www.fda.gov following the below link
REPORT HERE
2. Consumer Reporting Form FDA 3500B:

Follow the instructions on the form to either fax or mail it in for submission. For help filling out the form, see MedWatchLearn. The form is available at www.fda.gov following the below link

REPORT HERE
3. Call FDA at 1-800-FDA-1088 To Report By Telephone.
4. Reporting Form FDA 3500 Is Commonly Used By Health Professionals. The form is available at www.fda.gov following the below link
REPORT HERE

Additional Warning From The FDA Regarding Breast Implants:

VIEW FDA STATEMENT

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