MAUDE Adverse Event Report: ALLERGAN (COSTA RICA) STYLE 410 COHESIVE SILICONE GEL FILLED BREAST IMPLANT; PROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED

Catalog Number	FX-410450
Medical Device Problem Codes	Material Rupture (1546); Migration (4003)
Health Effect - Clinical Codes	Failure of Implant (1924); Swollen Lymph Nodes/Glands (4432)
Date of Event	08/15/2024
Type of Reportable Event	Serious Injury
Event or Problem Description
Patient reported "intra and extracapsular rupture, silicone migration as well as exchange from textured to smooth due to concern with the product".Healthcare professional later confirmed rupture.This record is for the left side.The device remains implanted.
Additional Manufacturer Narrative
A review of the device history record has been completed.No deviations or non-conformances noted.Further information from the reporter regarding event, product, or patient details has been requested.No additional information is available at this time.Reason for reoperation: rupture and silicone migration.
Additional Manufacturer Narrative
Additional, changed, and/or corrected data: a5, a6, b3, b5, d6b, h6.
Event or Problem Description
Patient reported "intra and extracapsular rupture, silicone migration as well as exchange from textured to smooth due to concern with the product".Later patient reported "reactive lymph nodes" and "silicone in two armpit lymph nodes and enlarged lymph nodes in breast area".Later healthcare professional reported "intracapsular (and extracapsular) rupture and implant exchange from textured to smooth".This record is for the left side.The device was explanted.
Additional Manufacturer Narrative
Additional, changed, and/or corrected data: b5, h6.The event of lymphadenopathy is a physiological complication and analysis of the device generally does not assist allergan in determining a probable cause for this event.
Event or Problem Description
Patient reported "intra and extracapsular rupture, silicone migration as well as exchange from textured to smooth due to concern with the product".Later patient reported "reactive lymph nodes" and "silicone in two armpit lymph nodes and enlarged lymph nodes in breast area".Later healthcare professional reported "intracapsular (and extracapsular) rupture and implant exchange from textured to smooth".Later patient reported "a lot of inflammation around the implant".This record is for the left side.The device was explanted.
Event or Problem Description
Patient reported "intra and extracapsular rupture, silicone migration as well as exchange from textured to smooth due to concern with the product".Later patient reported "reactive lymph nodes" and "silicone in two armpit lymph nodes and enlarged lymph nodes in breast area".Later healthcare professional reported "intracapsular (and extracapsular) rupture and implant exchange from textured to smooth".Later patient reported "a lot of inflammation around the implant".This record is for the left side.The device was explanted.
Additional Manufacturer Narrative
Additional, changed, and/or corrected data: d4, d.9, h.3, h4, h.6.Device evaluation: per the analysis performed, the assessments of the complaints and any potential manufacturing issue are displayed along with any further actions required: rupture and silicone migration: observed an opening through microscopic inspection assessed as unidentified (tear) opening.No further actions are required as it is not related to the manufacturing process.Anxiety - product/ procedure: unable to observe through visual inspection as it is a physiological phenomenon.Edema: unable to observe through visual inspection as it is a physiological phenomenon.None of the other observations performed during the device analysis (observed an creases and wear abrasion) are found to be potentially related to the manufacturing process, and, therefore, no further actions are required for these observations.

• Brand Name: STYLE 410 COHESIVE SILICONE GEL FILLED BREAST IMPLANT
• Common Device Name: PROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED
• Manufacturer (Section D): ALLERGAN (COSTA RICA); 900 parkway global park; zona franca; la aurora de heredia ; CS
• Manufacturer (Section G): ALLERGAN (COSTA RICA); 900 parkway global park; zona franca; la aurora de heredia ; CS
• Manufacturer Contact: terry ingram ; 2525 dupont drive; irvine, CA 92612 ; 8479366324
• MDR Report Key: 23023952
• Report Number: 9617229-2025-15413
• Device Sequence Number: 9455696
• Product Code: FTR
• UDI-Device Identifier: 10888628002999
• UDI-Public: (01)10888628002999(10)2713492(11)150305(17)200205
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: P040046
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Device Explanted Year: 2025
• Reporter Type: Manufacturer
• Report Source: Consumer,Health Professional
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 12/04/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 02/05/2020
• Device Catalogue Number: FX-410450
• Device Lot Number: 2713492
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 08/25/2025
• Supplement Date Received by Manufacturer: 09/13/2025; 10/29/2025; 11/17/2025
• Initial Report FDA Received Date: 09/11/2025
• Supplement Report FDA Received Date: 10/02/2025; 11/12/2025; 12/04/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 03/05/2015
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 64 YR
• Patient Sex: Female
• Patient Weight: 47 KG
• Patient Ethnicity: Non Hispanic
• Patient Race: White