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

Allergan PLC: Natrelle and McGhan Silicone-Filled Breast Implant BioCell Round Moderate Profile, Sterile, for the following style numbers: Style 110:110-090, 110-120, 110-150, 110-180, 110-210, 110-24

Is my product affected?

Natrelle and McGhan Silicone-Filled Breast Implant BioCell Round Moderate Profile, Sterile, for the following style numbers: Style 110:110-090, 110-120, 110-150, 110-180, 110-210, 110-240, 110-270, 110-300, 110-330, 110-360, 110-390, 110-420, 110-450, 110-480, 110-510; Style 115 :115-150, 115-167, 1

  • UPC 10888628002159
  • UPC 10888628002166
  • UPC 10888628002173
  • UPC 10888628002180
  • UPC 10888628002197
  • UPC 10888628002203
  • UPC 10888628002210
  • UPC 10888628002227
  • UPC 10888628002234
  • UPC 10888628002241
  • UPC 10888628002258
  • UPC 10888628002265
  • UPC 10888628002272
  • UPC 10888628002289
  • UPC 10888628002296
  • UPC 10888628002302
  • UPC 10888628002319
  • UPC 10888628002326
  • UPC 10888628002333
  • UPC 10888628002340
  • UPC 10888628002357
  • UPC 10888628002364
  • UPC 10888628002371
  • UPC 10888628002388
  • UPC 10888628002395
  • UPC 10888628002401
  • UPC 10888628002418
  • UPC 10888628002425
  • UPC 10888628002432
  • UPC 10888628002449
  • UPC 10888628002456
  • UPC 10888628002463
  • UPC 10888628002470
  • UPC 10888628002487
  • UPC 10888628002494
  • UPC 10888628002500
  • UPC 10888628002517
  • UPC 10888628002524
  • UPC 10888628002531
  • UPC 10888628002548

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

What happened

Allergan PLC is recalling Natrelle and McGhan silicone-filled breast implants with textured surfaces (BioCell Round Moderate Profile) in multiple style numbers 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 with textured breast implants. Approximately 4 million implants and tissue expanders combined have been distributed worldwide, including throughout all 50 U.S. states, U.S. territories, and eight other countries.

The affected implants are identified by specific style numbers (110, 115, and 120) and corresponding product codes/UDIs listed in the recall documentation. The source document does not specify what remedy is available to affected consumers, such as replacement, removal procedures, or compensation options.

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 110:110-090 10888628002159, 110-120 10888628002166, 110-150 10888628002173, 110-180 10888628002180, 110-210 10888628002197, 110-240 10888628002203, 110-270 10888628002210, 110-300 10888628002227, 110-330 10888628002234, 110-360 10888628002241, 110-390 10888628002258, 110-420 10888628002265, 110-450 10888628002272, 110-480 10888628002289, 110-510 10888628002296; STYLE 115:115-150 10888628002302, 115-167 10888628002319, 115-185 10888628002326, 115-203 10888628002333, 115-222 10888628002340, 115-253 10888628002357, 115-272 10888628002364, 115-290 10888628002371, 115-322 10888628002388, 115-354 10888628002395, 115-378 10888628002401, 115-401 10888628002418, 115-435 10888628002425, 115-469 10888628002432, 115-507 10888628002449, 115-547 10888628002456, 115-586 10888628002463, 115-627 10888628002470, 115-666 10888628002487, 115-716 10888628002494; STYLE 120:120-180 10888628002500, 120-220 10888628002517, 120-260 10888628002524, 120-300 10888628002531, 120-340 10888628002548, 120-400 10888628002555, 120-440 10888628002562, 120-500 10888628002579, 120-550 10888628002586, 120-600 10888628002593, 120-650 10888628002609;

Source

Official record: FDA (Device enforcement) ↗

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

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