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

Allergan PLC: Natrelle 133 Tissue Expanders w/Suture Tabs BIOCELL Full Height Variable Projection with MAGNA-FINDEr Xact & 21G Needle Infusion Set STYLE 133FV-T: 133FV-11-T, 133FV-12-T, 133FV-13-T, 13

Is my product affected?

Natrelle 133 Tissue Expanders w/Suture Tabs BIOCELL Full Height Variable Projection with MAGNA-FINDEr Xact & 21G Needle Infusion Set STYLE 133FV-T: 133FV-11-T, 133FV-12-T, 133FV-13-T, 133FV-14-T, 133FV-15-T, 133FV-16-T; STYLE 133MV-T: 133MV-11-T, 133MV-12-T, 133MV-13-T, 133MV-14-T, 133MV-15-T, 133MV

  • UPC 10888628004221
  • UPC 10888628004238
  • UPC 10888628004245
  • UPC 10888628004252
  • UPC 10888628004269
  • UPC 10888628004276
  • UPC 10888628004405
  • UPC 10888628004412
  • UPC 10888628004429
  • UPC 10888628004436
  • UPC 10888628004443
  • UPC 10888628004450
  • UPC 10888628004344
  • UPC 10888628004351
  • UPC 10888628004368
  • UPC 10888628004375
  • UPC 10888628004382
  • UPC 10888628004399
  • UPC 10888628004283
  • UPC 10888628004290
  • UPC 10888628004306
  • UPC 10888628004313
  • UPC 10888628004320
  • UPC 10888628004337
  • UPC 10888628004467
  • UPC 10888628004474
  • UPC 10888628004481
  • UPC 10888628004498
  • UPC 10888628004504
  • UPC 10888628004511
  • UPC 10888628004580
  • UPC 10888628004597
  • UPC 10888628004603
  • UPC 10888628004610
  • UPC 10888628004627
  • UPC 10888628004634
  • UPC 10888628004528
  • UPC 10888628004535
  • UPC 10888628004542
  • UPC 10888628004559

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

What happened

Allergan PLC is recalling Natrelle 133 tissue expanders with textured surfaces distributed worldwide, including all 50 U.S. states, U.S. territories, and several countries including Canada, Japan, and others. The recall encompasses approximately 4 million breast implants and tissue expanders across multiple styles and sizes. The recall 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 who have textured breast implants.

The affected products include multiple style variants (133FV-T, 133MV-T, 133LV-T, 133FX-T, 133MX-T, 133SX-T, and 133SV-T) in various sizes, identified by specific product codes and UDI numbers. Patients or healthcare providers who have these tissue expanders should reference the product codes provided to determine if they have an affected device. The source document does not specify a remedy or what affected consumers should do.

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 STYLE 133FV-T: 133FV-11-T 10888628004221, 133FV-12-T 10888628004238, 133FV-13-T 10888628004245, 133FV-14-T 10888628004252, 133FV-15-T 10888628004269, 133FV-16-T 10888628004276; STYLE 133MV-T: 133MV-11-T 10888628004405, 133MV-12-T 10888628004412, 133MV-13-T 10888628004429, 133MV-14-T 10888628004436, 133MV-15-T 10888628004443, 133MV-16-T 10888628004450; STYLE 133LV-T: 133LV-11-T 10888628004344, 133LV-12-T 10888628004351, 133LV-13-T 10888628004368, 133LV-14-T 10888628004375, 133LV-15-T 10888628004382, 133LV-16-T 10888628004399; STYLE 133FX-T: 133FX-11-T 10888628004283, 133FX-12-T 10888628004290, 133FX-13-T 10888628004306, 133FX-14-T 10888628004313, 133FX-15-T 10888628004320, 133FX-16-T 10888628004337; STYLE 133MX-T: 133MX-11-T 10888628004467, 133MX-12-T 10888628004474, 133MX-13-T 10888628004481, 133MX-14-T 10888628004498, 133MX-15-T 10888628004504, 133MX-16-T 10888628004511; STYLE 133SX-T: 133SX-11-T 10888628004580, 133SX-12-T 10888628004597, 133SX-13-T 10888628004603, 133SX-14-T 10888628004610, 133SX-15-T 10888628004627, 133SX-16-T 10888628004634; STYLE 133SV-T: 133SV-11-T 10888628004528, 133SV-12-T 10888628004535, 133SV-13-T 10888628004542, 133SV-14-T 10888628004559, 133SV-15-T 10888628004566 133SV-16-T 10888628004573

Source

Official record: FDA (Device enforcement) ↗

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

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