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

Catalog Number	SRX-420
Medical Device Problem Codes	Device Appears to Trigger Rejection (1524); Material Rupture (1546); Patient-Device Incompatibility (2682)
Health Effect - Clinical Codes	Capsular Contracture (1761); Foreign Body Reaction (1868)
Date of Event	12/23/2024
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
A review of the device history record has been completed.No deviations or non-conformance's noted.The events of "capsular contracture baker grade iv, pain and exposed implant" 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: rupture, capsular contracture baker grade iv, pain and exposed implant.
Event or Problem Description
Healthcare professional reported "rupture, capsular contracture baker grade iv, pain and exposed implant coming through the incision".This record is for the right side.Device remains implanted.
Event or Problem Description
Device was explanted.
Additional Manufacturer Narrative
Additional, changed, and/or corrected data: b5, b6, d9, h3, h6.Device evaluation: the device related to the reported events rupture, exposure, capsular contracture was received on april 29, 2025, with lot number 3590417.Based on the product analysis performed, the assessments of the complaint codes are: rupture: not observed.Exposure: unable to observe as it is not related to the manufacturing process.Capsular contracture: unable to observe as it is not related to the manufacturing process.As per the investigation procedure, deformation and creases were observed and none of the observations are found to be potentially related to the manufacturing process, no further actions are required.
Event or Problem Description
Healthcare professional reported "rupture, capsular contracture baker grade iv, pain and exposed implant coming through the incision".This record is for the right side.Device remains implanted.
Additional Manufacturer Narrative
Additional, changed, and/or corrected data: d6b.

• Brand Name: INSPIRA SMOOTH 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: 21812672
• Report Number: 9617229-2025-05944
• Device Sequence Number: 8990872
• Product Code: FTR
• UDI-Device Identifier: 10888628007512
• UDI-Public: (01)10888628007512(10)3590417(11)220208(17)270108
• Combination Product (Y/N): N
• Initial Reporter State: IN
• Initial Reporter Country: US
• PMA/510(K) Number: P020056
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2024
• Device Explanted Year: 2025
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 07/09/2025

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 Catalogue Number: SRX-420
• Device Lot Number: 3590417
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 03/17/2025
• Supplement Date Received by Manufacturer: 05/16/2025; 06/13/2025
• Initial Report FDA Received Date: 04/10/2025
• Supplement Report FDA Received Date: 06/12/2025; 07/09/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 02/08/2022
• 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: 41 YR
• Patient Sex: Female
• Patient Weight: 85 KG