The Recall Desk
HighFDA (Devices)·Z-2462-2019·Announced 2019-09-18

Allergan Recalls Textured Silicone-Filled Breast Implants Due to Lymphoma Risk

Allergan PLC is recalling specific textured silicone-filled breast implants and tissue expanders following FDA safety updates regarding a higher incidence of anaplastic large cell lymphoma (BIA-ALCL).

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a risk-of-harm product (medical device) associated with a serious condition (BIA-ALCL) where the source text does not explicitly report specific injuries or fatalities, fitting the 'High' severity criteria for risk-of-harm products where injury has not yet been reported.

Plain-English summary

Allergan PLC is recalling Natrelle and McGhan Silicone-Filled Breast Implants, TruForm 2 (Soft Touch), BIOCELL, Styles 110 Soft Touch and 120 Soft Touch. The recall covers 4,026,287 breast implants and tissue expanders combined. These products were used for breast augmentation and breast reconstruction.

The recall was initiated after the U.S. Food and Drug Administration (FDA) provided updated global safety information. This information indicates a higher incidence of anaplastic large cell lymphoma (BIA-ALCL) in patients who have textured breast implants. The affected products were distributed worldwide, including in all 50 U.S. states, the U.S. Virgin Islands, Puerto Rico, and several international locations.

Patients who have these specific textured breast implants should contact their healthcare provider to discuss the safety information and potential risks associated with BIA-ALCL.

The recalled product

Product
Natrelle and McGhan Silicone-Filled Breast Implants, TruForm 2 (Soft Touch), BIOCELL, Styles 110 Soft Touch and 120 Soft Touch Product Usage : Breast augmentation and Breast reconstruction
Manufacturer
Allergan PLC
Category
Medical Device — Breast Implants
Hazard
Affected units
4,026,287

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • All Lots: Note:This product was not distributed within the US

Distribution

Distributed nationwide across the United States.

The notice also names 52 states specifically:

Part of a larger recall action

This product is one of 15 recalled by Allergan PLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 15 products in this recall →

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