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

Model Number	SRLP-320
Medical Device Problem Codes	Device Appears to Trigger Rejection (1524); Material Rupture (1546)
Health Effect - Clinical Code	Capsular Contracture (1761)
Date of Event	02/13/2023
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 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.Further information from the reporter regarding event, product, or patient details has been requested.Reason for reoperation: rupture and capsular contracture baker grade unknown.
Event or Problem Description
Healthcare professional reported right side rupture confirmed with an ultrasound and capsular contracture baker grade unknown.Device remains implanted.
Additional Manufacturer Narrative
Device evaluation: based on the device analysis grid, the assessments of the complaint are: ¿ rupture: observed broken on radius side assessed as surgical impact opening and missing piece of shell assessed as inconclusive (shell thickness within specification).¿ capsular contracture: unable to observe as it is a medical event not related to the device.¿ inflammation/irritation: unable to observe as it is a medical event not related to the device.Additional observations: ¿ observed stress marks on the device.No further actions are required as the device was implanted.
Event or Problem Description
Healthcare professional reported right side rupture confirmed with an ultrasound and capsular contracture baker grade unknown.Healthcare professional later reported "capsular contracture, baker grade i/ii", ¿capsule with moderate chronic inflammation, foreign body giant cell reaction and fibrosis.¿ device has been explanted and not replaced.
Event or Problem Description
Device has been explanted.
Additional Manufacturer Narrative
Additional, changed, and/or corrected data: b5, d6b, h6.
Event or Problem Description
Healthcare professional later reported "capsular contracture, baker grade i/ii", ¿capsule with moderate chronic inflammation, foreign body giant cell reaction and fibrosis.¿ device has been explanted.
Additional Manufacturer Narrative
Additional, changed, and/or corrected data: b5, b6, d9, h3, h6 the event of capsular contracture is no longer reportable to the fda, as it is noted to be baker grade i/ii.

• 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
• Manufacturer (Section G): ALLERGAN (COSTA RICA); 900 parkway global park; zona franca
• Manufacturer Contact: terry ingram ; 12331-a riata trace parkway; building 3; austin, TX 78727 ; 8479366324
• MDR Report Key: 16499489
• Report Number: 9617229-2023-03298
• Device Sequence Number: 6611488
• Product Code: FTR
• UDI-Device Identifier: 10888628006911
• UDI-Public: 10888628006911
• Combination Product (Y/N): N
• Initial Reporter State: IL
• Initial Reporter Country: US
• PMA/510(K) Number: P020056
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Device Explanted Year: 2023
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 09/15/2023

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: 08/07/2020
• Device Model Number: SRLP-320
• Device Catalogue Number: SRLP-320
• Device Lot Number: 2798772
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 02/16/2023
• Supplement Date Received by Manufacturer: 05/09/2023; 07/26/2023; 08/22/2023
• Initial Report FDA Received Date: 03/07/2023
• Supplement Report FDA Received Date: 05/27/2023; 08/18/2023; 09/15/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 09/07/2015
• 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: 56 YR
• Patient Sex: Female
• Patient Weight: 79 KG