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

Model Number	SRLP-280
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	04/03/2023
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.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.
Event or Problem Description
Healthcare professional reported, left side rupture.The device remains implanted.
Event or Problem Description
Healthcare professional reported left side rupture.Healthcare professional additionally reported "capsule contracture", baker grade unknown, symptoms of breast implant illness - not related to the device, "stable groups of microcalcifications", and a hypoechoic mass - not related to the device.Healthcare professional later reported baker grade iv.The device has been explanted.
Additional Manufacturer Narrative
Additional, changed, and/or corrected data: h.6.Clarification to d9-date is when device photo was received.Photo analysis it is not possible to determine the lot number or catalog through the photos provided.Visual analysis of the photographs identified: ¿ rupture: observed, broken the device but cannot perform an assessment of the opening as no microscopic analysis can be performed.¿ capsular contracture: unable to observe as it is a medical event that is not related to the device.¿ calcification: no observed.¿ lump/nodule-ndr: not applicable as the event is not related to the device.¿ varied injuries -ndr: not applicable as the event is not related to the device.No additional observations.
Event or Problem Description
Device has been explanted.
Event or Problem Description
Healthcare professional additionally reported capsular contracture, baker grade unknown, symptoms of breast implant illness - not related to the device, "stable groups of microcalcifications", and a hypoechoic mass - not related to the device.Healthcare professional later reported capsular contracture, baker grade iv.
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.Reason for reoperation: capsular contracture, baker grade iv.

• 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: 17337306
• Report Number: 9617229-2023-11575
• Device Sequence Number: 15115240
• Product Code: FTR
• UDI-Device Identifier: 10888628006898
• UDI-Public: 10888628006898
• Combination Product (Y/N): N
• Initial Reporter State: NJ
• Initial Reporter Country: US
• PMA/510(K) Number: P020056
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2018
• Device Explanted Year: 2023
• Reporter Type: Manufacturer
• Report Source: Consumer,Health Professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 12/31/2023

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: 08/19/2022
• Device Model Number: SRLP-280
• Device Catalogue Number: SRLP-280
• Device Lot Number: 3106543
• 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: 06/27/2023
• Supplement Date Received by Manufacturer: 11/01/2023; 11/30/2023; Not provided
• Initial Report FDA Received Date: 07/17/2023
• Supplement Report FDA Received Date: 11/27/2023; 12/19/2023; 12/31/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 09/21/2017
• 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: 49 YR
• Patient Sex: Female
• Patient Weight: 56 KG