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

Model Number	TRF-345
Medical Device Problem Codes	Material Rupture (1546); Patient-Device Incompatibility (2682)
Health Effect - Clinical Codes	Capsular Contracture (1761); Swollen Lymph Nodes/Glands (4432)
Date of Event	06/15/2020
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
A review of the device history record has been completed.No deviations or non-conformances noted.The reported events are physiological complications and analysis of the device generally does not assist allergan in determining a probable cause for these events.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: "recall letter received, knot under armpit, low grade temp, implant feels hard that comes and goes, capsular contracture, and rupture".
Event or Problem Description
Patient reported right side "recall letter received" ,"knot under armpit", "implant feels hard that comes and goes".Patient additionally reported capsular contracture and rupture.Patient additionally reported "low grade temp", unrelated to the device.Device remains implanted.
Event or Problem Description
Patient reported right side "recall letter received" ,"knot under armpit", "implant feels hard that comes and goes".Patient additionally reported capsular contracture and rupture.Patient additionally reported "low grade temp", unrelated to the device.Device remains implanted.
Event or Problem Description
Patient later reported "swollen lymph nodes, contractures, ultrasound results show a snowstorm like appearance indicative of free silicone within the tissue that confirms that silicone has crossed over the capsule that is surrounding the implant".
Additional Manufacturer Narrative
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 later reported "swollen lymph nodes, contractures, ultrasound results show a snowstorm like appearance indicative of free silicone within the tissue that confirms that silicone has crossed over the capsule that is surrounding the implant".Device remains implanted.
Event or Problem Description
Device has been explanted.
Event or Problem Description
Patient reported right side "recall letter received" ,"knot under armpit", "implant feels hard that comes and goes".Patient additionally reported capsular contracture and rupture.Patient additionally reported "low grade temp", unrelated to the device.Device has been explanted.
Additional Manufacturer Narrative
Device evaluation: based on the device analysis grid, the assessments of the complaint are: ¿ rupture: observed 1 opening assessed as fold flow opening.¿ capsular contracture: unable to observe as it is not related to the device.¿ lymphadenopathy: unable to observe as it is not related to the device.¿ visibility/ palpability: unable to observe as it is not related to the device.¿ anxiety ¿ product/procedure: unable to observe as it is not related to the device.¿ lump/nodule: unable to observe as it is not related to the device.¿ fever ¿ ndr: unable to observe as it is not related to the device.¿ pain: unable to observe as it is not related to the device.No other observations observed.No further actions are required as no manufacturing issues are observed.Additional, changed, and/or corrected data: b5, d9, h3, h6.

• Brand Name: INSPIRA TEXTURED 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; CS
• Manufacturer (Section G): ALLERGAN (COSTA RICA); 900 parkway global park; zona franca; CS
• Manufacturer Contact: terry ingram ; 2525 dupont drive; building 3; irvine, CA 92612 ; 8479366324
• MDR Report Key: 10896476
• Report Number: 9617229-2020-19056
• Device Sequence Number: 3316052
• Product Code: FTR
• UDI-Device Identifier: 10888628008304
• UDI-Public: 10888628008304
• Combination Product (Y/N): N
• PMA/510(K) Number: P020056
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2024
• Reporter Type: Manufacturer
• Report Source: Consumer,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup,Followup,Followup
• Report Date (Section B): 06/17/2024

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?: No
• Operator of Device: Health Professional
• Device Expiration Date: 04/06/2021
• Device Model Number: TRF-345
• Device Catalogue Number: TRF-345
• Device Lot Number: 2909312
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 10/28/2020
• Supplement Date Received by Manufacturer: 01/10/2024; 01/23/2024; 03/25/2024; 04/30/2024; 06/13/2024
• Initial Report FDA Received Date: 11/24/2020
• Supplement Report FDA Received Date: 01/12/2024; 01/26/2024; 04/01/2024; 05/08/2024; 06/17/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 05/06/2016
• 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: 28 YR
• Patient Sex: Female