Natrelle breast implant for reconstruction

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The U. Food and Drug Administration today took significant action to protect women from breast implant-associated anaplastic large cell lymphoma BIA-ALCL by requesting that Allergan, the manufacturer of a specific type of textured implant, recall specific models of its textured breast implants from the U. The recall also includes tissue expanders used by patients prior to breast augmentation or reconstruction, including Natrelle Plus Tissue Expander and Natrelle Tissue Expander with Suture Tabs.

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On July 24,Allergan announced a global recall of Biocell textured breast implants and tissue expanders after the U. The recall comes after a rare type of cancer called anaplastic large-cell lymphoma ALCL has been linked to textured breast implants. Lymphoma is cancer of the lymphatic system.

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Today, the U. Food and Drug Administration FDA requested that Allerganthe manufacturer of a specific type of textured breast implant, recall specific models of its textured implants from the U. The recall also includes tissue expanders used by patients prior to breast augmentation or reconstruction, including Natrelle Plus Tissue Expander and Natrelle Tissue Expander with Suture Tabs.

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Individual results may vary. Follow natrellebreastaugmentation on Instagram. Follow natrellebreastreconstruction on Instagram.

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Skip navigation! Story from News. A little over two years ago, the Food and Drug Administration claimed that it had identified an association between textured breast implants and anaplastic large cell lymphoma, which is not a breast cancer but a rare type of non-Hodgkin's lymphoma that starts in white blood cells and is commonly referred to as BIA-ALCL.

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Food and Drug Administration in based on interim results from the Core Study; final year study results are now available. Seven hundred fifteen subjects were implanted with smooth and Biocell textured Natrelle round silicone implants and attended clinic visits at 0 to 4 weeks, 6 months, 1 year, and annually through 10 years. Approximately one-third of subjects underwent magnetic resonance imaging at years 1, 3, 5, 7, and 9 to assess rupture.

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Textured breast implants made by Allergan that have been linked to an unusual cancer are being recalled in the United States at the request of the Food and Drug Administrationand will also be recalled globally, the agency announced on Wednesday. The F. Worldwide, cases and 33 deaths from the cancer have been reported, with of the cases clearly attributed to Allergan Biocell implantsthe F.

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