Allergan recalls specific saline-filled breast implants due to higher risk of anaplastic large cell lymphoma (BIA-ALCL) in patients with textured 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.
Allergan is recalling certain saline-filled breast implants (Natrelle Biocell Full Height) that have a textured surface. These implants may carry a higher risk of a rare type of lymphoma called BIA-ALCL, which requires medical attention if the implant is still in place.
These textured implants can develop a rare lymphoma called BIA-ALCL. The condition occurs when the body's immune system reacts to the implant material, leading to fluid buildup and potential cancerous growths.
Women who received these specific implant styles for breast augmentation or reconstruction are affected. Those with textured implants are at higher risk for BIA-ALCL.
Check if your implant has a textured surface and matches the listed style numbers (e.g., 163-360CC, 168-120, 363LF-170, 468-195). Products may be sold under the Natrelle, McGhan, or Inamed brands.
Identify your implant's style number (e.g., 163-360CC, 168-120) to confirm if it's recalled.
Reach out to your surgeon or implant specialist to discuss potential removal or monitoring options.
The U.S. FDA updated safety information showing a higher incidence of BIA-ALCL (a rare lymphoma) in patients with textured breast implants.
The recall does not require immediate removal; consult your surgeon to determine if monitoring or removal is needed.
Recalled styles include 163-360CC, 168-120, 363LF-170, 468-195, and other specific combinations listed in the recall notice.
We’ve drafted a message you can send Allergan to request your refund or repair — edit it as you like.
Subject: Recall Z-2451-2019 — Allergan Allergan Hello, I own a Allergan that is covered by recall Z-2451-2019 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.
