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

Model Number	TCF-450
Medical Device Problem Code	Device Appears to Trigger Rejection (1524)
Health Effect - Clinical Code	Capsular Contracture (1761)
Type of Reportable Event	Serious Injury
Event or Problem Description
Healthcare professional reported right side capsular contracture baker grade iv as well as bilateral exchange of textured devices due to patient's concern with product.Device remains implanted.
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.No additional information is available at this time.Reason for reoperation: capsular contracture baker grade iv.
Event or Problem Description
Healthcare professional reported, right side capsular contracture, baker grade iv.As well as, bilateral exchange of textured devices, due to patient's concern with product.Device remains implanted.
Additional Manufacturer Narrative
Device evaluation:visual analysis of the returned device identified: weight to the spec, opening, brown particles on the surface of the shell.A microscopic analysis was performed which identify a striated edge opening.Based on the device analysis the final assessment is: - a striated edge opening on radius side assessed as surgical damage.
Event or Problem Description
Healthcare professional reported right side capsular contracture baker grade iv as well as bilateral exchange of textured devices due to patient's concern with product.Device has been explanted.
Additional Manufacturer Narrative
Correct reason for reoperation is: "biocell exchange".Additional, changed, and/or corrected data.
Event or Problem Description
The device was replaced.
Event or Problem Description
Healthcare professional reported right side capsular contracture baker grade iv as well as exchange of textured devices due to patient's concern with product.Device has been explanted.
Additional Manufacturer Narrative
Device photo analysis: visual analysis of the photographs identified a device appears to be intact, in the surface of the shell have red particles and red biological tissue next to device.The devices is labeled for right.Device analysis performed through photographs, due to the impossibility to perform microscopic analysis it is not possible to determine the most likely failure mode.Additional, changed, and/or corrected data: b5.

• Brand Name: INSPIRA TEXTURE 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
• 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: 13666125
• Report Number: 9617229-2022-02651
• Device Sequence Number: 5275672
• Product Code: FTR
• UDI-Device Identifier: 10888628031135
• UDI-Public: 10888628031135
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: P020056
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2022
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup,Followup,Followup
• Report Date (Section B): 11/27/2022

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: 10/29/2021
• Device Model Number: TCF-450
• Device Catalogue Number: TCF-450
• Device Lot Number: 2993989
• 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: 02/07/2022
• Supplement Date Received by Manufacturer: 05/20/2022; 06/15/2022; 08/04/2022; 11/09/2022
• Initial Report FDA Received Date: 03/04/2022
• Supplement Report FDA Received Date: 06/15/2022; 07/14/2022; 08/26/2022; 11/27/2022
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 11/29/2016
• 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 Sex: Female