enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Allergan Breast Implant Recalls | List of Affected Models

    www.drugwatch.com/allergan-breast-implants/recalls

    Allergan recalled its Biocell textured breast implants in 2019 due to a link to a rare cancer called BIA-ALCL. The FDA advises women with these implants to have them removed and provides a list of affected models.

  3. Breast Implant Recall: What You Need to Know | American ...

    www.cancer.org/cancer/latest-news/breast-implant...

    The FDA recalled Allergan Biocell textured breast implants and tissue expanders in 2019 due to a link with a rare lymphoma. Learn about the risks, symptoms, and what to do if you have recalled implants.

  4. FDA takes action to protect patients from risk of certain ...

    www.fda.gov/news-events/press-announcements/fda...

    The FDA has identified a link between Allergan BIOCELL textured breast implants and a rare type of cancer called BIA-ALCL. The agency has asked Allergan to voluntarily recall these products...

  5. Allergan Voluntarily Recalls BIOCELLĀ® Textured Breast ...

    www.fda.gov/safety/recalls-market-withdrawals...

    Allergan announces a global voluntary recall of BIOCELL® textured breast implants and tissue expanders due to the uncommon risk of breast implant-associated anaplastic large cell...

  6. An Update on BIA-ALCL: What Patients Should Know About ... - ABCS

    www.americanboardcosmeticsurgery.org/cosmetic...

    Allergan voluntarily recalled their BIOCELL textured breast implants in July 2019 due to increased risk of BIA-ALCL, a rare but serious condition. Learn about the recalled implant styles, the symptoms and treatment of BIA-ALCL, and the replacement warranty offered by Allergan.

  7. FDA issues warning letters to two breast implant ...

    www.fda.gov/news-events/press-announcements/fda...

    The FDA found that Allergan failed to comply with post-approval study requirements for two models of breast implants that were recalled due to increased risk of ALCL. The agency also warned Ideal...

  8. Class 1 Device Recall Natrelle Inspira, SiliconeFilled Breast ...

    www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/...

    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...