Allergan breast implant manufacturer

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Allergan is taking this action as a precaution following notification of recently updated global safety information concerning the uncommon incidence of breast implant-associated anaplastic large cell lymphoma BIA-ALCL provided by the U. Allergan will provide additional information to customers about how to return unused products. Patient safety is a priority for Allergan.

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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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Let friends in your social network know what you are reading about. Twelve women with Allergan textured implants died from breast implant-associated anaplastic large cell lymphoma, a rare cancer; many more diagnosed. A link has been sent to your friend's email address.

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The U. The move follows similar action in France, Australia, and Canada. Biocell implants feature a textured surface designed to prevent slippage and to minimize scar tissue.

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As more women have become ill or have died from a rare cancer linked to certain breast implantsAllergan has announced a voluntary worldwide recall of its textured implants. More than three dozen countries have already pulled that brand if implants. On Wednesday, the FDA announced there are now cases of BIA-ALCL worldwide and 33 people have died, a "significant increase" since the agency's last update earlier this year — reflecting new cases and 24 more deaths.

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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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The U. Food and Drug Administration FDA issued a recall this week of breast implants produced by pharmaceutical company Allergan, citing an increased risk of cancer among patients with implants manufactured by the company. Symptoms of the rare form of cancer include swelling and pain around the implant.

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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. The FDA also updated the number of worldwide cases of ALCL associated with breast implants: women have been diagnosed, and 33 women have died from the disease.

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Skip navigation! Story from Plastic Surgery. 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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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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