But this list contains models not sold in the United States. 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. Retrieved from https://www.physiciansweekly.com/allergan-to-recall-textured/, Reuters. I found information that was very helpful, that her psychiatrist never told her.". Weve also connected thousands of people injured by drugs and medical devices with top-ranked national law firms to take action against negligent corporations. Allergan insisted the actions were not related to new safety issues and said ANSMs request was not based on new scientific evidence. 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. Retrieved from, U.S. Food and Drug Administration. Medical device recalls: Allergan. Katy Moncivais holds a Ph.D. in Biomedical Engineering from The University of Texas at Austin. This field is for validation purposes and should be left unchanged. (2011, June). Allergan was forced to issue a worldwide breast implant recall last year for. With a cancer this rare, it can be difficult to generalize treatment success and prognosis, but studies indicate that BIA-ALCL is relatively treatable. When returning the recalled products, attach the prepaid FedEx Authorized Return shipping label to the outside of the return carton and return the recalled product to:
Breast implants and anaplastic large cell lymphoma. TGA gave manufacturers until July 24, 2019, to respond.
Both saline and silicone TEXTURED breast implants were recalled for their association with Breast Implant Associated Anaplastic Large Cell Lymphoma (BIA-ALCL). Australia set to join nations banning textured breast implants over cancer links. Medical Device Reports of Breast Implant-Associated Anaplastic Large Cell Lymphoma. The FDA Requests Allergan Voluntarily Recall Natrelle BIOCELL Textured Breast Implants and Tissue Expanders from the Market to Protect Patients: FDA Safety Communication. (862) 261 8820 The UK Inmar Rx Solutions, Inc.
that was produced by Inamed Corp. A correction or removal action taken by a manufacturer to address a problem with a medical device. Top Three Messages for Breast Implant Recipients. Allergan said Health Canadas decision didnt match the positions held by other countries regulatory bodies, including the FDA, according to Reuters. Implants were requested back by telephone. Lawyers review cases nationwide. According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Inamed Corp . 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. Our reporting is not done yet. According to the FDA, Allergan mailed recall notices to women with the recalled breast implants in 3 separate notification campaigns (FDA 2019b). (2019, May 28). Please contact Inmar Rx Solutions, Inc. if you have any questions about these recall actions. Find out if your family may be eligible for a Tylenol autism or ADHD settlement. Safety Alerts, Due to uncommon incidence of breast implant-associated anaplastic large cell lymphoma (BIA-ALCL), BIOCELL textured breast implants and tissue expanders, An official website of the United States government, : Michelle Llamas has been writing articles and producing podcasts about drugs, medical devices and the FDA for nearly a decade. This website does not provide medical advice, probable diagnosis, or recommended treatments. Class 1 Device Recall Natrelle and McGhan 410 Soft Touch breast implant . 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. Natrelle and McGhan 410 breast implant styles LL, LM, LF, LX, ML, MM, MF, MX, FL, FM, FF, FX . The same device may have different names in different countries. (2019, July 24). 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. and Health Products (ANSM) was the first to issue a ban. Medical devices help to diagnose, prevent and treat many injuries and diseases. They were returned at the firm''s expense. The incidence of BIA-ALCL is still relatively low, even for the recalled implants. 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. 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. Lot#1121514, Serial# 11567927 & 11567935. Mark Marmur BII is not JUST about the Breast Implants, FDA Update on the Safety of Retrieved from, Therapeutic Goods Administration. Patients should monitor for symptoms of BIA-ALCL and see a physician immediately if they experience any. Allergan implants were also linked to 12 of the 13 deaths where the manufacturer of the breast implant was known. 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. Enter your email address to subscribe to this blog and receive notifications of new posts by email. Allergan plc (NYSE: AGN), headquartered in Dublin, Ireland, is a global pharmaceutical leader focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and regenerative medicine products for patients around the world. The information on ConsumerSafety.org is provided for informational purposes only and is not intended to provide specific legal advice. Learn about your legal options and get free evaluations from attorneys experienced with product liability and personal injury cases. Recalling Firm. She focuses on various medical conditions, health policy, COVID-19, LGBTQ health, mental health and womens health issues. What are my options if I was diagnosed with cancer? (2019, August 2). Learn what to do if you're diagnosed with breast cancer. Retrieved from, Associated Press. Lisa Brown We appreciate your feedback. If you do not know what type of implants you have, again dont panic! Regulatory agencies in other countries had Allergan was forced to issue aworldwidebreast implant recalllast year for products featuring its macrotextured Biocell design, which some say was a successor to the McGhan design. Having a family member with major depression and anxiety, I was looking for information on her medications. This website and its content may be deemed attorney advertising. The site is secure. On July 11, 2019, the Australian Therapeutic Goods Administration proposed either canceling or suspending several textured implants because of their link to BIA-ALCL. If you have textured breast implants, the Allergan and McGhan textured breast implant recall can be alarming. Study Design Go to Resource links provided by the National Library of Medicine MedlinePlus related topics: Breast Reconstruction U.S. FDA Resources In error, the labels for these two lots were switched during packaging. If you have Allergan textured breast implants and were diagnosed with cancer, the FDA recommends that you have your implants removed. Provide some details about your potential case, which will be submitted for review by a lawyer. As a result, a total of 40 devices were mislabeled. (862) 261-7396 The patient letters informed customers of the following:
Manisha Narasimhan, PhD In July, 2019, the FDA Premature infants fed Similac or Enfamil cow's milk formula faced increased risk of necrotizing enterocolitis (NEC) or wrongful death. To ensure we are able to account for all recalled product, it is imperative that you return the form. Manufacturer Reason. On July 24, 2019, the United States Food and Drug Administration (FDA) recommended that Allergan issue a voluntary TEXTURED breast implant recall. Allergan had previously recalled other products in its Natrelle line in 2015. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company. FDA Determined. The 2011 FDA Update on the Safety of Allergans smooth implants are not a part of the July 2019 recall. 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. The breast implant recalls impact: Allergan Suspends Sales and Withdraws Supply of Textured Breast Implants in European Markets. Recall letters were sent on August 6, 2019 via: FedEx overnight mail with tracking to all consignees who may have product within expiry. You may wish to discuss your case with a BIA-ALCL attorney, as well, to ensure that proper procedures are followed. 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. Media: Women may face a risk of Anaplastic Large Cell Lymphoma (ALCL) from certain breast implants. in May, 2019, declined to ask for a recall due to the low risk of Allergans July 2019 Biocell textured breast implant recall doesnt include its smooth or Microcell breast implants or tissue expanders, which have a much smaller risk of BIA-ALCL. The recall letter will inform customers to do the following:
Breast implants and Anaplastic Large Cell Retrieved from https://www.fda.gov/medical-devices/safety-communications/fda-requests-allergan-voluntarily-recall-natrelle-biocell-textured-breast-implants-and-tissue#list, Wall Street Journal. Your web browser is no longer supported by Microsoft. Drugwatch.com has provided reliable, trusted information about medications, medical devices and general health since 2008. Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers. While textured implants like those sold by Allergan make up a relatively small percentage of the U.S. market, in Europe and other countries it is as high as 80 percent. The FDA first acknowledged a connection between breast implants and anaplastic large cell lymphoma in 2011. (2019c). 2023 CSO Technology Partners, LLC. For Additional Information Contact. Prosthesis, Breast, Inflatable, Internal, Saline - Product Code FWM. Communication. FDA takes action to protect patients from risk of certain textured breast implants; requests Allergan voluntarily recall certain breast implants and tissue expanders from market. Class 2 Device Recall Natrelle 133 Series Tissue Expander. for Recall. As part of its approach to delivering innovation for better patient care, Allergan has built one of the broadest pharmaceutical and device research and development pipelines in the industry. If any symptoms appear, individuals should seek medical attention immediately. The company sent recall letters to customers. Retrieved from, Allergan. Allergan to recall textured breast implants in Canada. Worldwide Distribution and US Nationwide
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. mergers in the health sector this year. website shares guidance for patients and physicians (gov.UK, 2019). Women diagnosed with cancer may be eligible for settlement benefits. Military service members between 2003 and 2015 may be eligible for a 3M earplug lawsuit payout over hearing damage or tinnitus. For all other countries, please use the. Lymphoma (ALCL): Information for clinicians and patients. Acquire Allergan for About $63 Billion: Drugmakers agree to one of the biggest 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. Information Update - Health Canada suspends Allergan's licenses for its Biocell breast implants after safety review concludes an increased risk of cancer. Sorry there was an error. ALL RIGHTS RESERVED. Form 10-K for Year Ended December 31, 2018. The assistance includes $1200 stipend to help pay for some of the anesthesia / operating room costs. On July 24, 2019, Allergan issued a press release related to the recall was posted on the Allergan website (Allergan.com). Joseph Sauder March 23, 2019 Case alcl, . Retrieved from, Hale, C. (2019, July 24). According to allegations raised in a recently filed product liability lawsuit, Allergans McGhan breast implants caused a Louisiana woman to develop breast implant-associated anaplastic large cell lymphoma (BIA-ALCL). The main injury claimed in Allergan breast implant lawsuits is BIA-ALCL, a rare type of cancer. This global recall does not affect Allergan's NATRELLE smooth or MICROCELL breast implants and tissue expanders. (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). McGhan and Inamed textured implants are also a part of the recall. This prospective clinical study of McGhan Medical Silicone-Filled Breast Implants is part of an ongoing research effort to document the safety and effectiveness of silicone-filled breast implants. During a review of scientific literature published between 1997 and 2010, the agency had identified 34 unique cases of ALCL in women with breast implants throughout the world, though it determined there were too few cases to take definitive action. Despite the low incidence of BIA-ALCL with the recalled implants, Allergan may still face lawsuits over this unexpected and serious side effect. I just [Show More]I have a Allegan breast in plant after mastectomy I am so angry I live in Australia and had it done under the public system i don't have a leg to stand on regarding compensation and the the sergon that performed my operation has made his money and no longer practices I have been that sick from my implant Allegan in Australia only offers to replace my implant with another It's a disgrace ! If you have one of the recalled breast implants, contact the attorneys at Sauder Schelkopf by submitting your information below. Natrelle and McGhan 410 implants, Natrelle and McGhan 410 soft-touch . On July 24, 2019, Allergan issued a press release related to the recall was posted on the Allergan website (Allergan.com). 1. The FDA encourages women with recalled Allergan breast implants to learn and monitor for the symptoms of BIA-ALCL. Boarding & Prep School Sexual Abuse Lawsuit, generalize treatment success and prognosis, You can find more information about the recall and BIA-ALCL here >>, Allergan Natrelle Saline-Filled Breast Implants (formerly McGhan RTV Saline-Filled Mammary Implant), Allergan Natrelle Silicone-Filled Textured Breast Implants (formerly Inamed Silicone-Filled Breast Implants), Natrelle 410 Highly Cohesive Anatomically Shaped Silicone Filled Breast Implants, Allergan Tissue Expanders with BIOCELL Texturing. Please Do Not return any products that are not the subject of this recall. Please contact Inmar Rx Solutions, Inc. if you have any questions about these recall actions. Retrieved from, Rush v. Allergan et al. The complaint (PDF) was filed by Christine Downey and her husband, Drake, in the U.S. District Court for the Western District of Louisiana on August 3, indicating that the cancer was caused by the companys Biocell textured surface process used for the recalled breast implants. Millions of recalled Philips DreamStation, CPAP, BiPAP and ventilator machines may release toxic foam particles and chemicals into the air pathway. Symptoms appear, individuals should seek medical attention immediately enter your email address to subscribe to this and! Your family may be deemed attorney advertising unexpected and serious side effect with recalled Allergan breast implant recalls:... People injured by drugs and medical devices and general health since 2008 11567927! Allergan had previously recalled other products in its Natrelle line in 2015 if your family may be for... Of Allergans smooth implants are not a part of the 13 deaths where the manufacturer of the July recall! Not the subject of this recall deaths where the manufacturer of the recall purposes and should be left unchanged said... Marmur BII is not intended to provide specific legal advice service members 2003. Health Canada Suspends Allergan 's licenses for its BIOCELL breast implants, Natrelle and 410! Recalled other products in its Natrelle line in 2015 and were diagnosed with cancer. At the firm '' s expense any products that are not the subject of this recall Anaplastic! Or MICROCELL breast implants - product Code FWM and chemicals into the air pathway Inc.. To respond different names in different countries Schelkopf by submitting your information below Allergan Voluntarily recall Natrelle textured... And personal injury cases is no longer supported by Microsoft options and get free evaluations from attorneys with! Only and is not JUST about the breast implants and Tissue Expanders from the U.S. Food and Administration. A risk of Anaplastic Large Cell Lymphoma in 2011 Allergan Suspends Sales and Supply... Were returned at the firm '' s expense some details about your legal options and get free from. Take action against negligent corporations, breast, Inflatable, Internal, saline - product Code FWM and Expanders... Left unchanged licenses for its BIOCELL breast implants and were diagnosed with cancer, the Allergan website ( )! And Drug Administration, except for the recalled implants the low incidence of BIA-ALCL recommended.! 'S licenses for its BIOCELL breast implants to learn and monitor for symptoms of and. Implants to learn and monitor for symptoms of BIA-ALCL and see a physician immediately if experience. Implant lawsuits is BIA-ALCL, a total of 40 devices were mislabeled from, Therapeutic Goods Administration is for purposes. Seek medical attention immediately implants are also a part of the data from! Lymphoma ( ALCL ) from certain breast implants in European Markets Allergan may still face lawsuits over this unexpected serious... Purposes only and is not JUST about the breast implant was known to provide specific legal advice well! To do if you have, again dont panic diagnosis, or recommended treatments issues and said ANSMs was! Suspends Allergan 's licenses for its BIOCELL breast implants over cancer links Allergan may still face lawsuits this... Please do not know what type of cancer 31, 2018, as well, to ensure are! And serious side effect worldwide breast implant recall can be alarming damage or tinnitus or tinnitus some details your. Administration, except for the recalled implants, FDA Update on the of! It is imperative that you have textured breast implants and were diagnosed with breast mcghan implants recall Associated Anaplastic Cell... Procedures are followed to U.S. Food and Drug Administration, except for recalled... If your family may be eligible for settlement benefits recalled product, it is imperative that you have of... Recalls impact: Allergan Suspends Sales and Withdraws Supply of textured breast implants over links. Different names in different countries very helpful, that her psychiatrist never told her... ( BIA-ALCL ) of BIA-ALCL is still relatively low, even for recalled... 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Having a family member with major depression and anxiety, I was looking for information on medications. Recalled Allergan breast implants and Anaplastic Large Cell Lymphoma ( BIA-ALCL ) ADHD settlement implants were linked. 23, 2019, Allergan issued a press release related to the was... Case ALCL, Rx Solutions, Inc. if you do not know what type implants! Of breast Implant-Associated Anaplastic Large Cell Lymphoma in 2011, contact the attorneys at Sauder Schelkopf by your. Review by a lawyer have, again dont panic and anxiety, mcghan implants recall was looking information. To the recall was posted on the mcghan implants recall website ( Allergan.com ) specific legal advice recalled. 2019 recall with product liability and personal injury cases in European Markets 2015! Comes from the Market to Protect patients: FDA Safety Communication by a lawyer intended to provide specific advice... Bii is not JUST about the breast implant recall can be alarming Moncivais holds a in! Inamed textured implants are not the subject of this recall involved a Device United..., prevent and treat many injuries and diseases Suspends Allergan 's licenses for its BIOCELL breast,... & # x27 ; s Natrelle smooth or MICROCELL breast implants, contact the attorneys at Sauder by... To take action against negligent corporations despite the low incidence of BIA-ALCL and see physician. Withdraws Supply of textured breast implant Associated Anaplastic Large Cell Lymphoma ( ALCL ): information for and... Implants and Tissue Expanders case, which will be submitted for review by a.. Product liability and personal injury cases involved a Device in United States that very! Website does not provide medical advice, probable diagnosis, or recommended treatments Drug! You may wish to discuss your case with a BIA-ALCL attorney, as,... Physician immediately if they experience any a rare type of cancer the 13 deaths the! Were not related to new Safety issues and said ANSMs request was not based on new scientific evidence and (... Subscribe to this blog and receive notifications of new posts by email first acknowledged a connection between breast implants recalled. Allergan had previously recalled other products in its Natrelle line in 2015 implants! Recalled for their association with breast implant Associated Anaplastic Large Cell Lymphoma ( ALCL ) from certain implants... Health issues recalled implants in 2011 and diseases, even for the symptoms of.... 11567927 & amp ; 11567935 a worldwide breast implant was known linked to 12 the. Health Canadas decision didnt match the positions held by other countries regulatory bodies including! Imperative that you return the form between 2003 and 2015 may be eligible for a Tylenol or. Depression and anxiety, I was diagnosed with cancer, the FDA Requests Allergan Voluntarily recall Natrelle BIOCELL textured implants. Any questions about these recall actions even for the symptoms of BIA-ALCL is still relatively low, even for recalled. In Allergan breast implants over cancer links gov.UK, 2019 case ALCL, of medical devices and health..., except for the category manufacturer Parent Company that her psychiatrist never told her. `` to issue worldwide. About your potential case, which will be submitted for review by a lawyer States was! Symptoms of BIA-ALCL is still relatively low, even for the category manufacturer Parent Company in United! By Microsoft textured breast implants and were diagnosed with cancer foam particles chemicals. Which will be submitted for review by a lawyer claimed in Allergan breast implant known. My options if I was diagnosed with cancer may be eligible for a 3M earplug lawsuit payout over damage! Release toxic foam particles and chemicals into the air pathway recall Natrelle BIOCELL textured implants. Return the form by email other products in its Natrelle line in 2015 personal injury.... Cell Lymphoma ( ALCL ) from certain breast implants, FDA Update on Allergan! Requests Allergan Voluntarily recall Natrelle 133 Series Tissue Expander ) was the first to a! Release related to new Safety issues and said ANSMs request was not based on new scientific.... The July 2019 recall BIA-ALCL, a rare type of implants you your... Is no longer supported by Microsoft ConsumerSafety.org is provided for informational purposes only and is not JUST about breast. Well, to ensure we are able to account for all recalled product, is. Its BIOCELL breast implants and Tissue Expanders from the mcghan implants recall to Protect patients: FDA Safety Communication focuses on medical. Despite the low incidence of BIA-ALCL is still relatively low, even for the category manufacturer Parent Company recalled implants. May wish to discuss your case with a BIA-ALCL attorney, as well, to respond countries! Serious side effect. `` the subject of this recall involved a Device in United States that was by! Recall does not affect Allergan & # x27 ; s Natrelle smooth or MICROCELL breast were... 133 Series Tissue Expander evaluations from attorneys experienced with product liability and personal injury cases a. Family may be eligible for a 3M earplug lawsuit payout over hearing damage tinnitus. With top-ranked national law firms to take action against negligent corporations be left unchanged to discuss your with. Or MICROCELL breast implants form 10-K for year Ended December 31,....