← Search recalls
FDA (Device enforcement)Recalled 2019-07-24class i

Allergan PLC: Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers: Style 163:163-360CC, 163-440CC, 163-530CC, 163-655CC, 163-780CC; Styl

Is my product affected?

Natrelle, Saline-Filled Breast Implant Biocell Full Height with Fill Tube, Sterile, for the following style numbers: Style 163:163-360CC, 163-440CC, 163-530CC, 163-655CC, 163-780CC; Style 168:168-120,168-150,168-180,168-210,168-240,168-270,168-300,168-330,168-360,168-390,168-420,168-450,168-480,168-

  • UPC 10888628000704
  • UPC 10888628000711
  • UPC 10888628000728
  • UPC 10888628000735
  • UPC 10888628000742
  • UPC 10888628000759
  • UPC 10888628000766
  • UPC 10888628000773
  • UPC 10888628000780
  • UPC 10888628000797
  • UPC 10888628000803
  • UPC 10888628000810
  • UPC 10888628000827
  • UPC 10888628000834
  • UPC 10888628000841
  • UPC 10888628000858
  • UPC 10888628000865
  • UPC 10888628000872
  • UPC 10888628000889
  • UPC 10888628000896
  • UPC 10888628000902
  • UPC 10888628000919
  • UPC 10888628000926
  • UPC 10888628000933
  • UPC 10888628000940
  • UPC 10888628000957
  • UPC 10888628000964
  • UPC 10888628000971
  • UPC 10888628000988
  • UPC 10888628000995
  • UPC 10888628001008
  • UPC 10888628001015
  • UPC 10888628001022
  • UPC 10888628001039
  • UPC 10888628001046
  • UPC 10888628001053
  • UPC 10888628001060
  • UPC 10888628001077
  • UPC 10888628001084
  • UPC 10888628001091

Check against the official notice below — it lists the full affected range.

What happened

Allergan PLC is recalling Natrelle saline-filled textured breast implants and tissue expanders across all lots and multiple style numbers (163, 168, 363, and 468) distributed worldwide and throughout the United States, including U.S. territories. The recall affects approximately 4 million implants and tissue expanders combined and was initiated following FDA notification of updated global safety information showing a higher incidence of anaplastic large cell lymphoma (BIA-ALCL), a type of cancer, in patients with textured breast implants.

The affected products were distributed nationwide across all 50 U.S. states plus the Virgin Islands and Puerto Rico, as well as internationally to Bermuda, Canada, Chile, Japan, Korea, Thailand, Taiwan, and Vietnam. The record does not specify a remedy or recommended course of action for affected consumers.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

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.

Details from the source

Reason for recall: 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. Distribution: Worldwide Distribution and US Nationwide All fifty (50) US States, the US Virgin Islands and Puerto Rico. (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). OUS: Bermuda, Canada, Chile, Japan, Korea, Thailand, Taiwan and Vietnam. Quantity: 4,026,287 Breast Implants and Tissue Expanders Combined in total Lot/code info: ALL LOTS Product Code/UDI Product Style 163: 163-360/10888628000704;163-440/10888628000711;163-530/10888628000728;163-655/10888628000735;163-780/10888628000742 Product Style 168: 168-120/10888628000759;168-150/10888628000766;168-180/10888628000773;168-210/10888628000780;168-240/10888628000797;168-270/10888628000803;168-300/10888628000810;168-330/10888628000827;168-360/10888628000834;168-390/10888628000841;168-420/10888628000858;168-450/10888628000865;168-480/10888628000872;168-510/10888628000889;168-550/10888628000896;168-600/10888628000902;168-650/10888628000919;168-700/10888628000926;168-750/10888628000933;168-800/10888628000940 Style 363: 363LF-170/10888628000957;363LF-200/10888628000964;363LF-230/10888628000971;363LF-260/10888628000988;363LF-300/10888628000995;363LF-330/10888628001008;363LF-370/10888628001015;363LF-410/10888628001022;363LF-450/10888628001039;363LF-510/10888628001046; 363LF-560/10888628001053;363LF-620/10888628001060;363LF-690/10888628001077; Style 468: 468-195/10888628001084;468-230/10888628001091;468-270/10888628001107;468-300/10888628001114;468-350/10888628001121;468-380/10888628001138;468-450/10888628001145;468-495/10888628001152;468-560/10888628001169;468-620/10888628001176

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

Related recalls

All FDA (Device enforcement) recalls

Hurt by this product? Start a free Case Check

ProductRisk is not a law firm and does not provide legal services or legal advice. ProductRisk is a free consumer product-safety information service operated by Plaintify, Inc., a technology company. If you ask to be connected with a law firm, any legal services are provided by that firm — not by ProductRisk or Plaintify.

Privacy · Plaintify