We only gather information from credible sources. (2018, December 19). Retrieved from, Lim, D. (2018, December 20). (2019, May 10). Attorney Advertising. Silicone Gel-Filled Breast Implants, https://www.drugwatch.com/allergan-breast-implants/lawsuits/, https://www.drugwatch.com/allergan-breast-implants/recalls/, https://www.drugwatch.com/news/2019/07/30/allergan-cites-rare-cancer-breast-implant-recall/, https://www.gov.uk/guidance/breast-implants-and-anaplastic-large-cell-lymphoma-alcl#history, https://www.physiciansweekly.com/allergan-to-recall-textured/, https://uk.reuters.com/article/us-allergan-recall/allergan-recalls-textured-breast-implants-worldwide-idUKKCN1UJ1N9, https://www.fda.gov/medical-devices/medical-device-recalls/allergan-recalls-natrelle-biocell-textured-breast-implants-due-risk-bia-alcl-cancer, https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?start_search=1&event_id=&productdescriptiontxt=&productcode=&IVDProducts=&rootCauseText=&recallstatus=¢erclassificationtypetext=&recallnumber=&postdatefrom=09%2F10%2F2019&postdateto=09%2F12%2F2019&productshortreasontxt=&firmlegalnam=Allergan&PMA_510K_Num=&pnumber=&knumber=&PAGENUM=500, https://www.fda.gov/medical-devices/safety-communications/fda-requests-allergan-voluntarily-recall-natrelle-biocell-textured-breast-implants-and-tissue#list, https://www.wsj.com/articles/abbvie-nears-deal-to-buy-allergan-for-more-than-60-billion-11561458504, Breast Reconstruction Options After Mastectomy, Removing the Entire Breast Implant Capsule. Allergans smooth implants are not a part of the July 2019 recall. With colleagues and commercial operations located in approximately 100 countries, Allergan is committed to working with physicians, healthcare providers and patients to deliver innovative and meaningful treatments that help people around the world live longer, healthier lives every day. The manufacturer took things a step further by promptly issuing a global recall of designated implants. Doctors diagnosed her with BIA-ALCL in 2017. Class 2 Device Recall Natrelle 133 Series Tissue Expander. The FDA indicates there are at least 573 known cases of BIA-ALCL diagnosed worldwide, including 33 deaths. Implants were requested back by telephone. BII is not JUST about the Breast Implants, FDA Update on the Safety of McGhan RTV Saline-Filled Mammary Implants became Allergan Natrelle Saline-Filled Breast Implants, and Inamed Silicone-Filled Breast Implants became Allergan Natrelle Silicone-Filled Textured Breast Implants. Unlike the textured implant recall, these recalls involved a relatively small number of devices. The recall letter will inform customers to do the following: Form 10-K for Year Ended December 31, 2018. With a cancer this rare, it can be difficult to generalize treatment success and prognosis, but studies indicate that BIA-ALCL is relatively treatable. A correction or removal action taken by a manufacturer to address a problem with a medical device. Retrieved from, U.S. Food and Drug Administration. (862) 261 8820 1. (2019c). Retrieved from, U.S. Food and Drug Administration. In December 2011, Downey began suffering pain and swelling in her left breast. The FDA says women who dont have symptoms of BIA-ALCL shouldnt remove their implants. Retrieved from, Associated Press. (862) 261-7396 International Consortium of Investigative Journalists. Recall of McGhan Round Breast Implant, Saline-Filled BIOCELL textured. DUBLIN, July 24, 2019/PRNewswire/ --Allergan plc (NYSE: AGN) today announced a voluntary worldwide recall of BIOCELLtextured breast implants and tissue expanders. Both saline and silicone TEXTURED breast implants were recalled for their association with Breast Implant Associated Anaplastic Large Cell Lymphoma (BIA-ALCL). Allergan issued a worldwide recall on July 24, 2019, but other countries had already asked the company to stop selling its implants because of BIA-ALCL concerns. Allergan said Health Canadas decision didnt match the positions held by other countries regulatory bodies, including the FDA, according to Reuters. Worldwide Distribution and US Nationwide Allergan had previously recalled other products in its Natrelle line in 2015. This information may be in your medical records, or you may have received it on a medical device card at the time of surgery. Lawyers review cases nationwide. (AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY). with breast implants may be more likely to be diagnosed with anaplastic large Typically, companies initiate a recall 4332 Empire Rd. In addition, Dr. Moncivais reviews portions of medically driven content to ensure scientific accuracy. Upon receipt of the Response Form, Inmar will issue Return Authorization label(s). Withdrawals, & To ensure we are able to account for all recalled product, it is imperative that you return the form. Lot#1121514, Serial# 11567927 & 11567935. Weve also connected thousands of people injured by drugs and medical devices with top-ranked national law firms to take action against negligent corporations. At the time the McGhan Breast Implants were placed into Christine Downeys body, she was not advised, nor did she have any independent knowledge, that the McGhan Breast Implants were anything other than safe, life-long products, the lawsuit notes. On average, women are diagnosed with BIA-ALCL approximately 9 years after receiving their implants, but time to diagnosis has ranged from 1 to 20 years in studies. All Rights Reserved. (2015, June 8). Find out if you may be eligible for a hearing loss settlement. Except as expressly required by law, Allergan disclaims any intent or obligation to update these forward-looking statements. Drugwatch.com is HONCode (Health On the Net Foundation) certified. 1. Allergan shipped expired products. If you have inventory of the recalled products, Quarantine product to prevent its use. risk of BIA-ALCL in 2011, updated in 2014, and in 2019. Allergan issues worldwide recall of textured breast implants over cancer cases. Cancer. Although Allergan allegedly knew about thebreast implant lymphoma riskfor years, the lawsuit notes that the only reason the implants are off the market is because the FDA forced the issue. 5. Allergan issued a worldwide recall of Biocell textured breast implants and tissue expanders that have been linked to a rare cancer. Health care providers may also perform a biopsy to test for cancer cells. Military service members between 2003 and 2015 may be eligible for a 3M earplug lawsuit payout over hearing damage or tinnitus. The information on Drugwatch.com has been medically and legally reviewed by more than 30 expert contributors, including doctors, pharmacists, lawyers, patient advocates and other health care professionals. FDA does not endorse either the product or the company. Manufacturer Reason. Manisha Narasimhan, PhD Not receiving a letter does NOT mean that your implants are not recalled. Actual results may differ materially from Allergan's current expectations depending upon a number of factors affecting Allergan's business. Assisting patients and their families since 2008. Complaint and Demand for Jury Trial. All fifty (50) US States, the US Virgin Islands and Puerto Rico. A former resident of Camp Lejeune has filed a lawsuit claiming water contamination on the base led to the development of breast cancer. This means recipients will need to maintain vigilance for symptoms for the lifetime of their breast implants. Patients should monitor for symptoms of BIA-ALCL and see a physician immediately if they experience any. Diagnosing BIA-ALCL usually involves MRIs and ultrasounds to check for fluid buildup and scar tissue. ALL RIGHTS RESERVED. https://www.fda.gov/medical-devices/safety-communications/breast-implants-reports-squamous-cell-carcinoma-and-various-lymphomas-capsule-around-implants-fda, https://www.fda.gov/medical-devices/breast-implants/medical-device-reports-breast-implant-associated-anaplastic-large-cell-lymphoma, https://www.fda.gov/medical-devices/safety-communications/fda-requests-allergan-voluntarily-recall-natrelle-biocell-textured-breast-implants-and-tissue, https://www.tga.gov.au/alert/breast-implants-and-anaplastic-large-cell-lymphoma, https://www.allergan.com/-/media/allergan/documents/us/Products/Biocell/Affected-Products-List.pdf, https://www.statnews.com/2019/07/24/allergan-recalls-textured-breast-implant-tied-to-rare-cancer/, https://www.fiercebiotech.com/medtech/allergan-issues-worldwide-recall-textured-breast-implants-over-cancer-cases, https://www.fda.gov/news-events/press-announcements/fda-takes-action-protect-patients-risk-certain-textured-breast-implants-requests-allergan, https://www.fda.gov/medical-devices/breast-implants/questions-and-answers-about-breast-implant-associated-anaplastic-large-cell-lymphoma-bia-alcl, https://www.icij.org/investigations/implant-files/australia-set-to-join-nations-banning-textured-breast-implants-over-cancer-links/, https://www.newswire.ca/news-releases/information-update-health-canada-suspends-allergan-s-licences-for-its-biocell-breast-implants-after-safety-review-concludes-an-increased-risk-of-cancer-880208806.html, https://www.reuters.com/article/us-allergan-canada/allergan-to-recall-textured-breast-implants-in-canada-idUSKCN1SY2BX, https://aboutlawsuits-wpengine.netdna-ssl.com/wp-content/uploads/2019-5-10-bia-alcl-rush-complaint.pdf, https://www.fda.gov/news-events/press-announcements/statement-binita-ashar-md-fdas-center-devices-and-radiological-health-agencys-continuing-efforts, https://allergan-web-cdn-prod.azureedge.net/actavis/actavis/media/allerganinvestors/financial-information/proxy-materials/2018_10-k.pdf, https://www.medtechdive.com/news/allergan-loses-ce-mark-for-textured-breast-implants-opening-eu-market/544885/, https://news.abbvie.com/news/allergan-press-releases/allergan-suspends-sales-and-withdraws-supply-textured-breast-implants-in-european-markets.htm, https://www.allergan.com/-/media/allergan/documents/us/Investors/FAQs/FAQonCEMarkNonRenewalofTexturedBreastImplantsandTexturedTissueExpandersBreastImplantsInvestorFAQs.pdf, https://www.icij.org/investigations/implant-files/allergan-textured-breast-implants-recalled-in-europe-pending-safety-review/, https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=137978, https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=137741, https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=137972, 163 BIOCELL Textured Shaped Full Height, Full Projection Saline Breast Implants, Natrelle 410 Highly Cohesive Anatomically Shaped Silicone-Filled Breast Implants, 410 LL, 410 LM, 410 LF, 410 LX, 410 ML, 410 MM, 410 MF, 410 MX, 410 FL, 410 FM, 410 FF, 410 FX, Biocell Textured Round Gel-Filled Implants, 110, 115, 120 Moderate, Midrange and High Projection, Natrelle Inspira Biocell Textured Responsive Silicone-Filled Breast Implants, Natrelle Inspira Biocell Textured Cohesive Silicone-Filled Breast Implants, Natrelle Biocelle Textured Soft Touch Silicone-Filled Breast Implants, Natrelle 133 Tissue Expanders with suture tabs. If you would like to speak with a Drugwatch representative, please call 888-645-1617, "Drugwatch opened my eyes to the realities of big pharmacy. Number in Commerce: 167 units total, 114 in the United States, Number in Commerce: 23 units total, 16 in the United States. Reports of BIA-ALCL began to surface in the late 1990s, but high-quality studies only became available in recent years, with the FDA reaching a determination of risk associated with Allergan implants just days ago. Acquire Allergan for About $63 Billion: Drugmakers agree to one of the biggest Premature infants fed Similac or Enfamil cow's milk formula faced increased risk of necrotizing enterocolitis (NEC) or wrongful death. Plaintiffs in Allergan breast implant lawsuits claim the manufacturer failed to warn of the risk of developing cancer. U.S. healthcare providers with questions regarding this announcement can contact Medical Information at 1-800-678-1605 option #2 or IR-Medcom@allergan.com. Natrelle 133 tissue expanders with and without suture tabs: styles 133FV, 133MV, 133LV, 133MX, 133SX, 133SV, T-133FV. Donate Advertisement Advertisement Advertisement Advertisement Advertisement Advertisement Advertisement Answer: How do we find out if our implants were part of the recall that just came out? Specific models of Allergan breast implants are associated with 6x greater risk of breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) versus other textured breast implants. The case joins dozens of similar class action lawsuits filed in recent months, as well as individual product liability complaints brought by women diagnosed with the breast implant lymphoma, which have beencentralized as part of a multidistrict litigation (MDL)in the federal court system. Regarding the financial assistance to return to the operating room to replace the implant -The breast implant companies offer financial assistance within 10 years from the date of implantation. experts (link to FDA testimony video) in the breast implant field. Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, St. 3 12/18/2019 Allergan PLC . We appreciate your feedback. Health Canada has suspended the licenses for Allergan's BioCell textured breast implants (the only macro-textured implants available in Canada), based upon the rare but serious risk of breast implant-associated anaplastic large cell lymphoma (BIA-ALCL), Allergan is voluntarily recalling Biocell breast implants as a precautionary measure. Frances National Agency for Safety of Medicines The patient letters informed customers of the following: One of our content team members will be in touch with you soon. Retrieved from, Allergan. OUS: Bermuda, Canada, Chile, Japan, Korea, Thailand, Taiwan and Vietnam. The compensation will vary depending on whether the patient has already been diagnosed with cancer or is choosing to have them removed as a preventative measure. (862) 261-7162 Keep a record of the device manufacturer, unique device identifier and implant model. CNN . Most implants are smooth. Drugwatch.com has provided reliable, trusted information about medications, medical devices and general health since 2008. (2019, May 28). Top Three Messages for Breast Implant Recipients. Patient letters were mailed on August 14, 19 and 26, 2019 to all impacted patients to which Allergan had complete names and addresses in their device tracking database. In a similar situation, manufacturers currently face numerous valsartan lawsuits from patients claiming they weren't warned of cancer as a possible side effect. Language Assistance Available: Espaol | | Ting Vit | | Tagalog | | | Kreyl Ayisyen | Franais | Polski | Portugus | Italiano | Deutsch | | | English. Having a family member with major depression and anxiety, I was looking for information on her medications. Following a number of attempts to identify the problem, she had the left saline breast implant removed in February 2012. Retrieved from https://www.drugwatch.com/allergan-breast-implants/lawsuits/, Drugwatch. In order to sell its breast implants in 33 European countries, Allergan needs a safety certificate known as a CE mark. 1 South Orange Ave, Suite 201, Orlando, FL 32801. Inamed Corp. 71 S Los Carneros Rd. Whether you are planning surgery, considering implants, or supporting a loved one, welcome! For Additional Information Contact. You may wish to discuss your case with a BIA-ALCL attorney, as well, to ensure that proper procedures are followed. (2019a). This global recall does not affect Allergan's NATRELLE smooth or MICROCELL breast implants and tissue expanders. United States McGhan BioDimensional Silicone-Filled Biocell Textured Breast Implants McGhan Magna-Site Tissue Expander McGhan Style 134 Croissant Shaped Tissue Expander Natrelle 133 Plus Issue Expanders Natrelle 133 Tissue Expanders with and without suture tabs Natrelle 410 Highly Cohesive Anatomically Shaped Silicone-Filled Breast Implants The FDA has linked Allergans textured breast implants, mostly those sold under the Natrelle brand, to a rare cancer called breast implant-associated anaplastic large cell lymphoma, or BIA-ALCL. The incidence of valsartan-associated cancer is lower than that of BIA-ALCL, so we may begin to see textured breast implant lawsuits filed in the very near future. Class 1 Device Recall Natrelle and McGhan 410 Soft Touch breast implant . Note: If you need help accessing information in different file formats, see Allergan cites rare cancer as reason for Women diagnosed with cancer may be eligible for settlement benefits. Allergan implants were also linked to 12 of the 13 deaths where the manufacturer of the breast implant was known. McGhan and Inamed textured implants are also a part of the recall. If you do not know what type of implants you have, again dont panic! (2019, July 24). What are my options if I was diagnosed with cancer? Michelle collaborates with experts, including board-certified doctors, patients and advocates, to provide trusted health information to the public. BIOCELLsaline-filled and silicone-filled textured breast implants and tissue expanders will no longer be distributed or sold in any market where they are currently available. Retrieved from https://www.fda.gov/medical-devices/medical-device-recalls/allergan-recalls-natrelle-biocell-textured-breast-implants-due-risk-bia-alcl-cancer, U.S. Food and Drug Administration (FDA). Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health. Withdrawn Affected Product Names and Styles. Conduct a physical count of the affected products in your possession and record the count on the enclosed Recall Stock Response Form. +44 7725 758677 The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of anaplastic large cell lymphoma (BIA-ALCL) in patients who have textured breast implants. Side effects of Tylenol may cause autism and ADHD among children exposed during pregnancy. All fifty (50) US States, the US Virgin Islands and Puerto Rico. The FDA is not recommending women have the breast implants removed if they are showing no symptoms. The main injury claimed in Allergan breast implant lawsuits is BIA-ALCL, a rare type of cancer. After analyzing hundreds of adverse event reports of BIA-ALCL, regulators found certain Allergan implants to carry six times higher risk of BIA-ALCL than other textured breast implants. breast implants in Canada. FDA Determined. Allergan released a list of all its recalled textured breast implant products sold across the globe. Allergan BIA-ALCL is a relatively rare type of cancer affecting a small percentage of all women with breast implants. Class 1 Device Recall Natrelle and McGhan SiliconeFilled Breast Implants. (862) 261-7320, View original content to download multimedia: http://www.prnewswire.com/news, More Recalls, Market Retrieved from, Allergan. If you have inventory of the recalled products, Quarantine product to prevent its use. Silicone Gel-Filled Breast Implants stated that Women In October 2019, after noticing an enlargement in one of her breast implants, she was diagnosed with BIA-ALCL. cell lymphoma (ALCL), (Drugwatch, 2019b, FDA, 2011). Retrieved from, U.S. Food and Drug Administration. If you have Allergan textured breast implants and were diagnosed with cancer, the FDA recommends that you have your implants removed. A Tennessee woman has filed a product liability lawsuit that indicates Allergan McGhan breast implants caused cancer to develop in the tissue surrounding implant, known as breast. 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.S. Food and Drug Administration (FDA). Leukemia, lymphoma and other cancer may be caused by benzene in Neutrogena, Aveeno, Coppertone and other sunscreens. How, 4,026,287 Breast Implants and Tissue Expanders Combined in total. Some women may choose to have breast reconstruction using another implant or their own fat tissue. In July, 2019, the FDA Of those, 481 have been linked to Biocell breast implant designs. 6. Because many women have breast implants with a smooth surface, which have NOT been linked to BIA-ALCL, the overall percentage of all women with implants diagnosed with BIA-ALCL is small. (2011, June). (2019, June 25). In its Allergan recall announcement, the FDA noted that "the risk of BIA-ALCL with Allergan BIOCELL textured implants is approximately 6 times the risk of BIA-ALCL with textured implants from other manufacturers marketing in the U.S." Other sources estimate the risk to be even higher. The action was initiated following notification by the U.S. FDA of their recently updated, global safety information concerning the higher incidence of anaplastic large cell lymphoma (BIA-ALCL) in patients who have textured breast implants. (2019, July 24). BIA-ALCL. U.S. Food and Drug Administration. It starts with our strict sourcing guidelines. 01:39 - Source: CNN. (2018, December 31). The site is sponsored by law firms. I just won't it removed. In the United Kingdom, the UK.gov Language Assistance Available: Espaol | | Ting Vit | | Tagalog | | | Kreyl Ayisyen | Franais | Polski | Portugus | Italiano | Deutsch | | | English, Prosthesis, breast, noninflatable, internal, silicone gel-filled, Instructions for Downloading Viewers and Players, Class 1 Device Recall Natrelle and McGhan 410 Soft Touch breast implant, Natrelle and McGhan 410 TruForm 2 (Soft Touch) BIOCELL breast implant, Styles LL, LM, LF, ML, MM, MF, FL, FM, FF, All Lots: Note:This product was not distributed within the US. You may wish to begin researching breast explant options, because waiting lists for qualified surgeons are quite long. Prior results do not predict a similar outcome. Join our newsletter to stay up to date on dangerous drugs and devices, keep up on lawsuit and settlement news, learn about FDA recalls, and more. Natrelle and McGhan Round Gel Implants . At the first sign of persistent swelling or pain around the implants, women should speak to their health care providers and undergo tests for BIA-ALCL. In late 2018, French regulatory agency Agence Nationale de Scurit du Mdicament (ANSM) requested Allergan recall its textured breast implants and tissue expanders from European markets. For the hundreds of thousands of women who get breast implants yearly, news that a rare cancer may be associated with their implants can be understandably scary. Information Update - Health Canada suspends Allergan's licenses for its Biocell breast implants after safety review concludes an increased risk of cancer. Recalling Firm. (AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY). FDA RECALL OF NATRELLE BREAST IMPLANTS On July 24, 2019 Allergan and the FDA announced a recall, after an investigation confirmed that Allergan Biocell textured breast implants were linked to a higher cancer risk than any other type of breast implant. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. (2019). Textured shells allow tissue to grow into the surface of the implant and keep it in place. Textured implants from McGhan Medical are also included in the recall. 1. Class 2 Device Recall Natrelle Re-sterilizable Breast Implant Sizer, Size: 410 cc. Allergan will provide additional information to customers about how to return unused products. Language Assistance Available: Espaol | | Ting Vit | | Tagalog | | | Kreyl Ayisyen | Franais | Polski | Portugus | Italiano | Deutsch | | | English, Prosthesis, Breast, Inflatable, Internal, Saline, Code of Federal Regulations (CFR) Title 21 7.55, PMAs with Product Code = FWM and Original Applicant = Allergan, Instructions for Downloading Viewers and Players, Class 3 Device Recall McGhan Style 163360cc SalineFilled BIOCELL textured Breast Implants, McGhan Style 163-360cc Saline-Filled BIOCELL textured Breast Implants, Catalogue Number :163-360. 1. Please read our disclaimer for more information about our website. Retrieved from, U.S. Food and Drug Administration. UPDATE: On June 1, 2020, Allergan issued a press release outlining a dedicated multi-channel campaign to contact women who may not be aware of the Biocell recall and to improve tracking information for U. S. Breast Implant patients (link: https://news.abbvie.com/news/press-releases/allergan-aesthetics-launches-dedicated-multi-channel-campaign-to-contact-patients-who-may-not-be-aware-biocell-recall-and-to-improve-tracking-information-for-us-breast-implant-patients.htm) Send the Recall Stock Response Form to Inmar Rx Solutions, Inc via fax or email within five (5) business days of receipt. Skilled in adult stem cells, medical devices, biomechanics, bacterial and mammalian cell culture, and regenerative medicine, she provides guidance on an array of topics affecting consumers. Worldwide Distribution and US Nationwide FDA Home; Medical Devices; Databases - 510(k) | DeNovo . U.S. data is current through June 2018. Upon receipt of the Response Form, Inmar will issue Return Authorization label(s). Keep people safe from potentially harmful drugs, medical devices and procedures by informing them of medical conditions, severe side effects and ways to take action. Women who received Allergan textured implants should know the symptoms of BIA-ALCL and monitor their health. The recalled breast implants represent less than 5 percent of implants sold in the United States. Shes an experienced Regenerative Medicine Consultant with a demonstrated history of working in the hospital & healthcare industry. 3. The 2011 FDA Update on the Safety of The site is secure. I had a nurse from a plastic surgeons office tell me that because I did not receive a letter, my implants were not recalled. Review our editorial policy to learn more about our process for producing accurate, current and balanced content. However, as required by the new California Consumer Privacy Act (CCPA), you may record your preference to view or remove your personal information by completing the form below. Drugwatch.com partners with law firms. The company sent recall letters to customers. Allergan manufactured smooth and textured implants until the FDA found the company's Biocell textured implants had a higher risk of breast implant-associated anaplastic large cell lymphoma. document.getElementById( "ak_js_2" ).setAttribute( "value", ( new Date() ).getTime() ); Provide additional contact information if you want an attorney to review your comments and contact you about a potential case. Instructions for Downloading Viewers and Players. Do you work in the medical industry? Fort Worth, TX 76155 Conduct a physical count of the affected products in your possession and record the count on the enclosed Recall Stock Response Form. We will direct you to one of our trusted legal partners for a free case review. This week the U.S. Food & Drug Administration (FDA) announced that Allergan textured breast implants had been tied to the development of breast implant-associated anaplastic large cell lymphoma (BIA-ALCL), a rare form of cancer. The move came after the US Food . Retrieved from, U.S. Food and Drug Administration. On July 24, 2019, Allergan issued a press release related to the recall was posted on the Allergan website (Allergan.com). 714-246-4500. If your breast implant is on the recall list and you have no symptoms, the FDA does not recommend that you remove your implants.
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