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

Model Number	MM-410450
Medical Device Problem Code	Patient-Device Incompatibility (2682)
Health Effect - Clinical Code	Capsular Contracture (1761)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
A review of the device history record has been initiated.If any new, changed or corrected information is noted, a supplemental medwatch will be submitted.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: anxiety around product and capsular contracture baker grade unknown.
Event or Problem Description
Patient reported "anxiety with textured implants".Healthcare professional reported capsular contracture baker grade unknown.Device remains implanted.
Event or Problem Description
Device has been explanted.
Event or Problem Description
Events occurred on left side device.Patient representative reported ¿mental anguish¿ and ¿pain.¿ patient representative also reported patient ¿suffered personal injuries and related damages¿ and ¿suffering;¿ these events are not device related.

• 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; CS
• MDR Report Key: 10288930
• Report Number: 9617229-2020-12396
• Device Sequence Number: 16934554
• Product Code: FTR
• UDI-Device Identifier: 10888628003668
• UDI-Public: 10888628003668
• Combination Product (Y/N): N
• Initial Reporter State: IN
• PMA/510(K) Number: P040046
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2014
• Device Explanted Year: 2020
• Reporter Type: Manufacturer
• Report Source: consumer,health professional
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 03/25/2021

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: 09/22/2019
• Device Model Number: MM-410450
• Device Catalogue Number: MM-410450
• Device Lot Number: 2666765
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 06/17/2020
• Supplement Date Received by Manufacturer: 08/06/2020; 02/26/2021
• Initial Report FDA Received Date: 07/17/2020
• Supplement Report FDA Received Date: 09/01/2020; 03/25/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention