Allergan Breast Implant Lawsuit
Breast augmentation has long been a popular cosmetic procedure for women seeking to enhance their appearance and boost their self-confidence. However, in recent years, concerns have emerged surrounding the safety of breast implants, particularly those manufactured by Allergan. Several lawsuits over Allergan breast implant, like Allergan breast implant lawsuit and Allergan breast implants cancer lawsuit, have gained significant attention as individuals affected by adverse health conditions, including breast cancer, seek justice and compensation for their suffering.
Allergan Breast Implants
Allergan breast implants are medical devices used for breast augmentation or reconstruction surgeries. They are made of a silicone outer shell filled with either saline solution (saline-filled implants) or silicone gel (silicone-filled implants). Allergan, a leading pharmaceutical company, has been manufacturing breast implants for several years.
Allergan breast implants have been widely used for two primary purposes: breast augmentation and breast reconstruction. Breast augmentation is a cosmetic procedure aimed at enhancing the size and shape of the breasts for aesthetic purposes. On the other hand, breast reconstruction is a surgical procedure performed after a mastectomy or to correct congenital deformities, aiming to restore the natural appearance of the breasts.
Allergan breast implants have been favored by many patients and surgeons due to their durability, natural feel, and aesthetic results. They have been used by individuals seeking breast enhancement or restoration, catering to different body types and desired outcomes.
Allergan Breast Implant Recall
In recent years, the safety of textured breast implants manufactured by Allergan has been called into question, leading to a significant event in the medical community — the Allergan breast implant recall. This recall was initiated as a precautionary measure to address concerns regarding the potential risks associated with certain models of Allergan textured breast implants.
On July 24, 2019, at the request of the US Food & Drug Administration (FDA), Allergan undertook a voluntary recall of its products. The FDA highlighted a potential link between Allergan Biocell® breast implants and an increased risk of cancer. Specifically, the recalled breast implants have been associated with the development of breast implant-associated anaplastic large cell lymphoma (BIA-ALCL).
Recalled Allergan Breast Implant Products
The FDA requested Allergan to recall specific models of their textured breast implants to address potential risks and ensure patient safety, including:
- Natrelle Saline-Filled Textured Breast Implants
- Natrelle Silicone-Filled Textured Breast Implants
- Natrelle 410 Highly Cohesive Anatomically Shaped Silicone-Filled Textured Breast Implants
- Natrelle Inspira Responsive Silicone-Filled Textured Breast Implants
- Natrelle BioCell Textured Breast Implants
- Natrelle 133 Plus Tissue Expander
- Natrelle 133 Tissue Expander with Suture Tabs
- McGhan BioDimensional Silicone-Filled Biocell Textured Breast Implants
- McGhan Magna-Site Tissue Expander
- McGhan Style 134 Croissant-Shaped Tissue Expander
- Style 133 Biospan Tissue ExpanderAge-related macular degeneration
Reasons Behind the Allergan Breast Implant Recall
- Potential Link to BIA-ALCL: The recall was prompted by the potential association between Allergan textured breast implants and the development of a rare lymphoma called BIA-ALCL.
- Safety Concerns: Concerns about the safety of Allergan textured breast implants prompted the recall, as studies indicated a higher risk of complications compared to smooth-surfaced implants.
- Regulatory Agency Request: Regulatory agencies, including the FDA, requested Allergan to recall specific models of their textured breast implants to address potential risks.
- Risk Mitigation: The recall aimed to minimize potential harm by removing the identified textured breast implants from circulation.
- Patient Safety Priority: Allergan prioritized patient safety by proactively recalling the textured implants and addressing the concerns associated with their use.
Adverse Effects of Allergan Breast Implants
- Breast Implant-Associated Anaplastic Large Cell Lymphoma (BIA-ALCL)
- Implant rupture or leakage
- Capsular contracture
- Implant displacement or malposition
- Infection
- Pain or discomfort in the breast area
- Changes in breast shape or appearance
- Scarring or changes in nipple sensation
- Breast asymmetry
- Need for implant removal or revision surgery
Allergan Breast Implants and Cancer
The potential link between Allergan breast implants and cancer, particularly Breast Implant-Associated Anaplastic Large Cell Lymphoma (BIA-ALCL), has raised significant concerns within the medical community and among individuals who have received these implants. While BIA-ALCL is not breast cancer itself, it is a rare form of lymphoma that affects the tissue surrounding the breast implant and can lead to severe complications.
The prevalence of BIA-ALCL associated with Allergan breast implants in the United States has been the subject of investigation and monitoring by regulatory agencies, such as the FDA. According to data reported by the FDA, the risk of developing BIA-ALCL associated with Allergan textured breast implants ranges from approximately 1 in 2,207 to 1 in 86,029 individuals with these implants. The reported cases of BIA-ALCL have primarily occurred in individuals who have received textured breast implants rather than smooth-surfaced implants.
Symptoms of BIA-ALCL
The symptoms of BIA-ALCL caused by Allergan breast implants can vary from person to person. If you have Allergan breast implants and experience any of the following symptoms, it is crucial to seek medical attention:
- Unexplained swelling or enlargement of one or both breasts, which may occur years after the initial breast implant surgery.
- Pain or discomfort in the breast area that persists or worsens over time, not related to injury or trauma.
- The accumulation of fluid around the breast implant, causing pain, swelling, or a lump in the breast or armpit.
- Changes in the shape, size, or symmetry of the breasts, such as asymmetry or visible deformities.
- The development of a rash or changes in the texture of the skin on or around the breast.
- The presence of palpable lumps, masses, or nodules in the breast or armpit region.
Allergan's Response to the Product Recall
In response to the concerns surrounding the potential link between their textured breast implants and BIA-ALCL, Allergan voluntarily recalled specific models of their textured implants as a precautionary measure. This recall aimed to prioritize patient safety and minimize potential harm.
Due to the potential risk of BIA-ALCL, individuals who have received Allergan textured breast implants are advised to remain vigilant and informed about the latest updates and recommendations from regulatory agencies and healthcare providers. Regular monitoring and follow-up appointments with healthcare professionals specializing in breast health are recommended to detect any potential signs or symptoms of BIA-ALCL.
Allergan Breast Implant Lawsuits: Cancer-Related Complications
Individuals impacted by Allergan breast implants are taking legal action to seek recourse for the alleged connection between these implants and cancer. Various types of Allergan breast implant lawsuit have emerged in response to these concerns, including the following:
- Allergan Breast Implant Cancer Lawsuits: These lawsuits focus on establishing the connection between Allergan breast implants and the increased risk of cancer, such as BIA-ALCL.
- Allergan Class Action Lawsuit Breast Implants: Affected individuals are pursuing Allergan implant class action lawsuits over harm or complications related to Allergan breast implants.
- Allergan Implant Recall Lawsuits: Related to the Allergan implant recall and aim to address the alleged harm caused by the use of Allergan textured implants.
- Allergan Textured Implant Lawsuits: Focus on the alleged risks and defects associated with Allergan’s textured implants.
- By seeking legal recourse, plaintiffs aim to secure compensation for medical expenses, pain and suffering, lost wages, and other damages caused by the alleged connection between Allergan breast implants and cancer.
Allergan Breast Implant Lawsuits: Legal Implications
As individuals impacted by these implants pursue legal remedies for alleged harm and complications, Allergan breast implants have faced a surge of lawsuits. These lawsuits shed light on various legal aspects and potential outcomes.
The top allegations in Allergan breast implant lawsuit include:
- Product Liability: Allergan’s breast implants were defectively designed, manufactured, or labeled, resulting in increased risks and complications.
- Failure to Warn: Allergan neglected to provide adequate warnings regarding the potential risks and complications associated with their breast implants.
- Negligence: Allergan breached its duty of care by producing and distributing unsafe breast implants.
- Fraudulent Misrepresentation: Allergan engaged in deceptive practices by misrepresenting the safety and risks of their breast implants.
- Breach of Warranty: Allergan violated express or implied warranties by providing faulty breast implants.
Allergan implant lawsuits carry significant legal implications that can profoundly impact both the plaintiffs and the manufacturer. They include:
- Product Liability Standards: Implications surrounding compliance with product liability standards for defective design, manufacturing, or labeling of Allergan breast implants.
- Causation and Medical Evidence: Establishing a causal link between Allergan breast implants and alleged harm through medical evidence, expert testimonies, and scientific studies.
- Class Action Certification: Consolidating multiple claims into a single Allergan implant lawsuit, potentially leading to significant settlements or judgments.
- Settlements and Compensation: Resolving Allergan implant recall lawsuits through settlements to provide compensation for damages and avoid prolonged litigation.
- Precedent Setting: Establishing legal precedents that influence industry standards and future litigation involving similar products or claims.
- Regulatory Impact: Potential changes to safety regulations, further investigations, or new requirements for medical device manufacturers as a result of the Allergan breast implant lawsuit.
Is the Allergan Breast Implant Recall a Lawsuit?
No, the Allergan breast implant recall is not a lawsuit itself. It is a proactive measure taken by Allergan and regulatory authorities to ensure patient safety. However, individuals affected by Allergan breast implants still need to pursue legal action through Allergan breast implant lawsuit to seek compensation for their injuries, medical expenses, emotional distress, and other damages.
Bring an Allergan Breast Implant Lawsuit
Allergan breast implant cancer lawsuits demand immediate attention. The allegations surrounding Allergan breast implants are serious, the consequences are profound, and justice must be sought. Ethen Ostroff Law understands the urgency of these cases. We partner with specialized firms nationwide to fight for the rights of those affected by Allergan breast implants and ensure they receive the representation they deserve.
If you or a loved one has suffered harm or complications due to Allergan breast implants, act now.
What are you waiting for? Contact Ethen Ostroff Law now at 610-510-8883 ( by calling this number, you consent to receive SMS updates from Ethen Ostroff Law) or Submit Form to get free consultation.
