MAUDE Adverse Event Report: ALLERGAN (COSTA RICA) STYLE 410 COHESIVE SILICONE GEL FILLED BREAST IMPLANT; PROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED

Model Number	MF-410640
Medical Device Problem Code	Device Appears to Trigger Rejection (1524)
Health Effect - Clinical Code	Capsular Contracture (1761)
Date of Event	12/03/2019
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.No additional information is available at this time.Reason for reoperation: "concern with the product," "a lump on left breast", "left transaxiliary is numb", "chest pain", "feels something moving down left arm", capsular contracture baker grade unknown.
Event or Problem Description
Patient reported exchange of textured breast implants due to concern with the product, "a lump on left breast", "left transaxiliary is numb", "chest pain", and "feels something moving down left arm." patient additionally reported "cancer survivor"; this is not device related.Healthcare professional later reported capsular contracture baker grade unknown.Device has been explanted.
Event or Problem Description
Patient reported exchange of textured breast implants due to concern with the product, "a lump on left breast", "left transaxiliary is numb", "chest pain", and "feels something moving down left arm." patient additionally reported "cancer survivor"; this is not device related.Healthcare professional later reported capsular contracture baker grade unknown.Device has been explanted.
Additional Manufacturer Narrative
Correction: aware date of initial medwatch should have been 11/jul/2022.This was date we first became aware of reportable event and matches the parent record aware date.Device evaluation: the device related to the reported event of anxiety-product/procedure, lump/nodule, pain, sensation increase/decrease, neurological symptoms and capsular contracture was received on july 29, 2022, with lot number 2830357.Analysis of the returned device identified the weight the device within specification, red particles in the shell, crease fold and encapsulation.Cloudy and voids in the gel observed after autoclave cycle.Based on the device analysis the final assessment is: no issues found related with the manufacturing.

• Brand Name: STYLE 410 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: 15161344
• Report Number: 9617229-2022-13694
• Device Sequence Number: 5812305
• Product Code: FTR
• UDI-Device Identifier: 10888628003521
• UDI-Public: 10888628003521
• Combination Product (Y/N): N
• Initial Reporter State: VA
• Initial Reporter Country: US
• PMA/510(K) Number: P040046
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2022
• Reporter Type: Manufacturer
• Report Source: Consumer,Health Professional
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 08/31/2022

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: 10/12/2020
• Device Model Number: MF-410640
• Device Catalogue Number: MF-410640
• Device Lot Number: 2830357
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 12/13/2019
• Supplement Date Received by Manufacturer: 08/09/2022
• Initial Report FDA Received Date: 08/03/2022
• Supplement Report FDA Received Date: 08/31/2022
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 11/12/2015
• 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: 61 YR
• Patient Sex: Female