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

Catalog Number	SCM-485
Medical Device Problem Codes	Device Appears to Trigger Rejection (1524); Material Rupture (1546)
Health Effect - Clinical Codes	Capsular Contracture (1761); Failure of Implant (1924)
Date of Event	07/02/2025
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Device evaluation: based on the product analysis performed, the assessments of the complaint codes are: ¿ rupture: not observed.¿ capsular contracture: unable to observe as it is not related to the manufacturing process.As per the investigation procedure, deformation, wear abrasion, voids and crease 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" confirmed via ultrasound.Later healthcare professional reported "capsular contracture baker grade unknown".Later healthcare professional reported "baker grade iv".This record is for the left side.Device was explanted and replaced.Device will be returned.
Event or Problem Description
Healthcare professional reported rupture confirmed via ultrasound.This record is for the left side.Device was explanted and replaced.
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.
Additional Manufacturer Narrative
The event of capsular contracture is a physiological complication and analysis of the device generally does not assist allergan in determining a probable cause for this event.Additional, changed, and/or corrected data: a5, a6, b5, h6.
Event or Problem Description
Healthcare professional reported "rupture" confirmed via ultrasound.Later healthcare professional reported "capsular contracture baker grade unknown".Later healthcare professional reported "baker grade iv".This record is for the left side.Device was explanted and replaced.Device will be returned.
Additional Manufacturer Narrative
Additional, changed, and/or corrected data: b5, b6, g2.
Event or Problem Description
Healthcare professional reported "rupture" confirmed via ultrasound.Later healthcare professional reported "capsular contracture".Later healthcare professional reported "baker grade iv".Later patient reported "intracapsular rupture" and "stepladder sign".This record is for the left side.Device was explanted.

• Brand Name: INSPIRA SMOOTH 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: 23125119
• Report Number: 9617229-2025-16105
• Device Sequence Number: 18079892
• Product Code: FTR
• UDI-Device Identifier: 10888628029941
• UDI-Public: (01)10888628029941(10)3357311(11)190715(17)240615
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: P020056
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Device Explanted Year: 2025
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 02/18/2026

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: 06/15/2024
• Device Catalogue Number: SCM-485
• Device Lot Number: 3357311
• 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: 09/08/2025
• Supplement Date Received by Manufacturer: 09/24/2025; 10/27/2025; 01/30/2026
• Initial Report FDA Received Date: 09/23/2025
• Supplement Report FDA Received Date: 10/15/2025; 11/17/2025; 02/18/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 07/15/2019
• 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: 59 YR
• Patient Sex: Female
• Patient Weight: 50 KG