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Poly Implant Prothèse (PIP) was a brand of breast implants manufactured by a French company of the same name, which became widely known for its use of non-medical grade silicone gel in its implants. Introduced in the 1990s, PIP implants were marketed as providing a safe and effective option for breast augmentation and reconstruction. However, the implants faced significant scrutiny and controversy due to concerns about the safety of their silicone gel, which was later found to be of inferior quality and not approved for medical use. The primary issue with PIP implants was the use of substandard silicone gel, which increased the risk of implant rupture and leakage. This compromised the integrity of the implants and raised serious health concerns for those who received them. The gel inside PIP implants was more prone to leakage, leading to potential health risks, including breast pain, swelling, and, in severe cases, the need for surgical removal of the implants. Complications associated with PIP implants included higher rates of implant rupture and leakage compared to other breast implants. Patients may experience symptoms such as breast pain, lumps, or changes in breast shape. In some cases, the leakage of the silicone gel could lead to localized inflammation or infection. Following the revelations about the safety issues with PIP implants, regulatory agencies and health organizations recommended the removal of these implants and ongoing monitoring of affected patients. Despite the serious concerns, the case of PIP implants led to increased scrutiny and regulation of breast implant safety and quality standards.