Allergan recalls Natrelle 410 textured breast implants due to higher risk of BIA-ALCL. Affected models include LL, LM, LF, LX, ML, MM, MF, MX, FL, FM, FF, FX styles. Contact for removal or replacement.
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.
Allergan is recalling Natrelle 410 textured breast implants because they may cause a rare type of lymphoma called BIA-ALCL. This recall affects specific implant styles sold under Natrelle, McGhan, or Inamed brands.
Textured breast implants can sometimes cause a rare type of lymphoma called BIA-ALCL. This condition is linked to the textured surface of the implant, which may lead to an immune response that forms cancerous tissue.
Women who have received Natrelle 410 textured breast implants are most at risk. These implants were sold for breast augmentation and reconstruction.
Check if your implant is labeled with style numbers like LL-410135, LM-410140, or LF-410125. Products may have been sold under Natrelle, McGhan, or Inamed brands.
Reach out to Allergan for guidance on removing or replacing the implant.
The recall does not require immediate removal. Affected users should contact Allergan for advice on next steps.
BIA-ALCL stands for Breast Implant-Associated Anaplastic Large Cell Lymphoma, a rare type of lymphoma linked to textured breast implants.
No, only specific textured Natrelle 410 models with style numbers listed in the recall are affected.
We’ve drafted a message you can send Allergan to request your refund or repair — edit it as you like.
Subject: Recall Z-2452-2019 — Allergan Allergan Hello, I own a Allergan that is covered by recall Z-2452-2019 from Allergan. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
