U.S. flag An official website of the United States government
  1. Home
  2. Medical Devices
  3. Products and Medical Procedures
  4. Implants and Prosthetics
  5. Breast Implants
  6. Medical Device Reports for Systemic Symptoms in Women with Breast Implants
  1. Breast Implants

Medical Device Reports for Systemic Symptoms in Women with Breast Implants

A number of patients and clinicians use the term “breast implant illness” or “BII” to describe a variety of systemic symptoms which may be reported by some women following reconstruction or augmentation with breast implants. They include, but are not limited to, fatigue, problems with memory or concentration (“brain fog”), joint and muscle pain, hair loss, weight changes and anxiety/depression. The appearance of such symptoms has been reported with all types of breast implants regardless of filling, shape or surface characteristic, and their onset anywhere from immediately after implantation to years later.  Although some women report improvement or resolution of symptoms following removal of the implants, the cause of the symptoms and the degree to which they may be related to the implants are unclear at the current time. Research continues to be performed to better understand any potential association with breast implants. Currently, however, BII is not recognized as a formal medical diagnosis and there are no specific tests or recognized criteria to define or characterize it.

FDA conducted a query of the MDR database for all reports posted between January 1, 2008 and October 31, 2019 referring to a saline- or silicone-filled breast prosthesis whose event narrative included one or more of the terms listed in Appendix A, or one of the following terms or phrases:

  • BII
  • Breast implant illness
  • Generalized/unexplained illness
  • Unexplained systemic symptoms.

It is important to note that while the MDR system is a valuable source of information, it is a passive surveillance system with significant limitations, including incomplete, inaccurate, untimely, unverified, or biased data in the reports. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting, duplicate reporting of events, and the lack of information about the total number of breast implants. Furthermore, the receipt of an MDR does not itself establish or confirm that the device caused or contributed to the adverse event or symptom reported. Concurrent medications or devices, habits and known or unrecognized patient comorbidities or conditions may confound the ability to draw a definitive conclusion regarding causality in individual cases.

After eliminating apparent duplicate reports, FDA’s query identified a total of 3,577 MDRs meeting the established search criteria. However, missing information limited our ability to identify all potential duplicate reports.  The majority (70%) of the MDRs were received from October 2018 to October 2019.

Information related to the age of the patient was available in 1,998 of the 3,577 reports (56%). The average age cited in these reports was 43 years of age with a range of 9-88 years. Several MDRs were submitted for children born to women with breast implants where the reporter believed the symptoms or events to be attributable to the mother’s implants.

For 75% of the MDRs (2,675/3,577), enough information was provided to determine the time from device implantation to the onset of the stated systemic symptoms. In these cases, the average time to onset was 4.9 years with a range of 0 - 42.5 years.

Table 1 provides the top 10 most frequent systemic-related search terms appearing in the 3,577 reports.

Table 1. Most Common Systemic Signs or Symptoms

Symptom Percentage of MDRs (N=3,577)
Fatigue 49%
“Brain Fog” 25%
Joint Pain 25%
Anxiety 24%
Hair Loss 21%
Depression 19%
Rash 18%
Autoimmune Diseases* 18%
Inflammation 18%
Weight Fluctuation 18%

* Any mention of autoimmune disease which can includes symptoms of, or diagnosis of autoimmune diseases

Of the 3,577 MDRs, 1535 (or 43%) reported the patient undergoing device explant at some time following the onset of symptoms. Of these, 1,473 reports provided information sufficient to calculate the time from implantation to explant. The average time to explant was 9 years, with a range of 0- 47 years. Only 290 MDRs provided information related to the status of a woman’s symptoms following explant. Of these, 279 noted improvement and 11 noted either no improvement or worsening of symptoms.

FDA will continue to monitor MDRs and provide updates as warranted.

Appendix A. Search terms relevant to systemic symptoms referred to as BII

acid reflux easy bruising inflammation premature aging
adrenal EBV insomnia rash
allergy fibromyalgia intolerana Raynaud
allergies fog joint reflux
anxiety frequent urination joint pain rheumatoid arthritis
arthritis gallbladder kidney scleroderma
autoimmune gastritis leaky gut shortness of breath
candida Fatigue libido SIBO
chest discomfort fever liver sick
choking gastrointestinal issues lupus sinus
cold Lyme disease Sjogren
connective tissue GERD memory loss sleep
cough GI issues menopause slow healing
dehydration hair loss metallic taste slow muscle recovery
depression Hashimoto migraine throat clearing
difficulty swallowing headaches multiple sclerosis thyroid
heart pain tingling
dry eyes heart palpitations muscle pain toxic
dry hair heart rate night sweats toxic shock
dry skin hormone numbness urinary tract
dying hysterectomy pancreatitis vertigo
ear ringing IBS panic attack weight
early menopause illness parathyroid yeast

a Use of the * wildcard will capture all words that begin with “intoleran”, including intolerance and intolerant


Back to Top