The FDA has published millions upon millions of reports about medical device problems. The agency allows manufacturers to submit reports about problems with their products to its employees. The agency makes these reports publically accessible through its MAUDE database. Several factors can affect implant safety. For example, a textured surface can prevent rotation. A woman who smokes has a greater chance of complications from implants. Be sure to check your medical history for autoimmune diseases if you are considering breast implants.
Textured surfaces prevent rotation
Tough surfaces, however, will prevent the rotation of breast implants that are teardrop-shaped. Because textured surfaces have a Velcro-like effect, they will prevent rotation of the implant. Round implants won't rotate as much and will therefore be more secure in breast pockets. Though rotation of teardrop-shaped implants is a small risk, it can still be an aesthetic issue.
Avoiding autoimmune disorders
FDA has not yet concluded if silicone implants in breasts can be linked to autoimmune conditions. Some doctors have reported developing arthritis-like disorders after breast implants. While there hasn't been any conclusive evidence from the FDA linking breast implants to autoimmune disorders, there are growing signs. A recent World Health Organization study found a connection between breast implants & rare cancers.
Surgery can be reversed
Breast implant surgery cannot be reversed, unlike cosmetic procedures like tummy tuck or rhinoplasty. Your breast will never regain its original shape once implants have been in place. Implanted breast tissue can become dimpled or wrinkled. This procedure can also result in significant pain. You can reduce these risks by hiring a trained plastic surgeon in breast implant surgery.
Patient device cards
Updates to FDA's guidelines regarding patient device cards (for breast implants) have made it more crucial than ever to provide information about the product to patients. The FDA has updated its guidelines to require that patient device cards contain information about the type of implant and serial number as well any boxed warnings. Patients should be able to access additional information by using web links on the cards.
Examining for rupture
The Food and Drug Administration advises regular imaging of breast implants after two to three year. Ultrasound is able to distinguish between normal and broken implants. Normal implants will appear well-defined and homogeneous on ultrasound. Implants that have been damaged will appear like a snowstorm. An MRI should be scheduled if you have any of these symptoms. This will allow you to determine the extent of the rupture. This type if imaging is not covered by any health insurance.