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The U.S. Food and Drug Administration (FDA) has requested that pharmaceutical company Allergan recall its BIOCELL textured breast implants due to a risk of breast implant\u2013associated anaplastic large cell lymphoma (BIA-ALCL), according to an announcement from the agency.
Certain breast implants Manufactured by the pharmaceutical company Allergan have been recalled for posing health and safety risks. The implants were recalled, in part, due to their link to breast implant-associated anaplastic large-cell lymphoma, or BIA-ALCL.
Brothers offers both Allergan\u2122 and Mentor® implants for your breast enhancement. It is crucial to note that both Allergan\u2122 and Mentor® are FDA-approved brands that adhere to the highest standards of safety in manufacturing, testing, and clinical trials.
To submit a claim For coverage eligibility, your surgeon must contact the Allergan Product Surveillance team prior to surgery at 1-800-624-4261 and provide the appropriate documentation. The surgeon is required to return the explanted, disinfected Natrelle® breast implant(s) within 3 months of the date of explantation.
Breast Implant Tracking is Required by Law It is required by federal law that breast implant manufacturers track all of their implants with a serial number. Following your breast implant surgery, board certified plastic surgeon Dr.
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The U.S. Food and Drug Administration (FDA) requires that all breast implant manufacturers include identification information with each implant. This is so the vast number of implants produced can be tracked, helping to monitor patients' long-term safety.
The recall also extends to other BIOCELL breast implants, including: Natrelle saline-filled breast implants, Natrelle silicone-filled breast implants, Natrelle Inspira silicone-filled breast implants, and Natrelle 410 highly cohesive anatomically shaped silicone-filled breast implants.
They are approved for breast augmentation in women age 22 or older and for breast reconstruction in women of any age. They are also used in revision surgeries, which correct or improve the result of an original surgery.
Microchip implant tracking would allow for correct selection of those patients who need to have surgical re-operation in case of implant failure or of device recall for safety reasons. In addition to breast implants, microchips could be also be used in other medical devices outside the field of plastic surgery.
Signs That Your Breast Implants Have Shifted Your breasts either look visually different from left to right or feel different to the touch; Your breasts were symmetrical right after surgery, but are now asymmetrical; Your nipples show out of the top of a bra or bikini top; and/or.

allergan device tracking