MAUDE Adverse Event Report: MENTOR TEXAS MENTOR MEMORYSHAPE BREAST IMPLANT; PROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED

Model Number	3341409
Medical Device Problem Code	Migration (4003)
Health Effect - Clinical Code	Wrinkling (2613)
Date of Event	10/21/2020
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
At the time of this report, mentor has received no information regarding explantation or an expected explantation date.It is unknown at this time if the device will be made available for return.As a result, no product failure analysis can be conducted, and no determination of possible contributing factors can be made.As such, the investigation will be closed.If the complaint device is received in the future, the investigation will be reopened and conducted as appropriate.A manufacturing record evaluation (mre) was performed, and no anomalies were found related to this complaint.In addition, the mre verifies that the device was manufactured in accordance with documented specification and procedures.Reason for device explant and/or reoperation: wrinkling, implant malposition/displacement.Manufacturer¿s reference number: (b)(4).
Event or Problem Description
It was reported that a caucasian female patient, who's undergone breast reconstruction, as part of a clinical study, with two 555cc mentor memoryshape breast implants on (b)(6) 2020 , suffered bilateral breast wrinkling, post-procedure.On (b)(6) 2020 , the patient underwent bilateral breast surgical intervention (fat grafting) and the issues were resolved.However, on (b)(6) 2020 , the patient was then diagnosed with bilateral implant malposition/displacement.The patient underwent an unspecified surgical intervention to resolved that issue on an unspecified date.At the time of this report, mentor has received no information regarding explantation or an expected explantation date.A supplemental report will be submitted if clarifying information is received.This medwatch form is for the right breast prosthesis.
Additional Manufacturer Narrative
On december 28, 2021, mentor became aware that the suspect medical devices were implanted for breast reconstruction revision.Manufacturer¿s reference number: (b)(4).
Additional Manufacturer Narrative
On january 20, 2022, mentor became aware that the onset of the patient's implant malposition/displacement was on (b)(6) 2020.

• Brand Name: MENTOR MEMORYSHAPE BREAST IMPLANT
• Common Device Name: PROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED
• Manufacturer (Section D): MENTOR TEXAS; 3041 skyway circle north; irving TX 75038
• Manufacturer (Section G): MENTOR TEXAS; 3041 skyway circle north; irving TX 75038
• Manufacturer Contact: gabriel alfageme ; 3041 skyway circle north; irving, TX 75038 ; 9497898687
• MDR Report Key: 11932313
• Report Number: 1645337-2021-06210
• Device Sequence Number: 14293490
• Product Code: FTR
• UDI-Device Identifier: 00081317005117
• UDI-Public: 00081317005117
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: P060028
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Study,User Facility
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 05/12/2021

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?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 04/21/2021
• Device Model Number: 3341409
• Device Catalogue Number: 3341409
• Device Lot Number: 7317003
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 05/12/2021
• Supplement Date Received by Manufacturer: 12/28/2021; 01/20/2022
• Initial Report FDA Received Date: 06/03/2021
• Supplement Report FDA Received Date: 01/21/2022; 02/01/2022
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 04/21/2016
• 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 Age: 64 YR
• Patient Sex: Female
• Patient Weight: 74 KG
• Patient Ethnicity: Non Hispanic
• Patient Race: White