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

Model Number	3341404
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Pain (1994); Deformity/ Disfigurement (2360); Wrinkling (2613); Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available (4581)
Date of Event	10/13/2020
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, asymmetry.Mentor is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which mentor has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, mentor, or its employees that the report constitutes an admission that the device, mentor, or its employees caused or contributed to the potential event described in this report.Manufacturer¿s reference number: (b)(4).
Event or Problem Description
It was reported that a caucasian female patient who underwent a breast reconstruction procedure with mentor memoryshape breast implant 680cc gel breast prostheses developed wrinkling and asymmetry in both breasts post implantation.As a result, the patient underwent an unspecified surgical intervention on (b)(6) 2020.This medwatch report is for the patient¿s left breast prosthesis.
Additional Manufacturer Narrative
On 05-apr-2023, mentor received additional information about the event.It was reported that following the surgical intervention on (b)(6) 2020, the patient was dissatisfied with the appearance of her breasts.As a result, the patient underwent fat grafting and scar revision procedures on (b)(6) 2021.H6 health effect - clinical code e2402: patient dissatisfaction with procedure outcome manufacturer¿s reference number: (b)(4).
Additional Manufacturer Narrative
On 12-may-2023, mentor received additional information about the event.The patient developed pain in her right breast post implantation.This medwatch report is for the patient¿s left breast prosthesis.Manufacturer¿s reference number: (b)(4).
Additional Manufacturer Narrative
On 14-aug-2023, mentor received additional information about the event.It was reported that the patient developed left-side pain post implantation.This medwatch report is for the patient¿s left breast prosthesis.Manufacturer¿s reference number: (b)(4).
Additional Manufacturer Narrative
On 03-oct-2025, mentor received additional information about the event.The patient presented with osteoporosis of the left hip with pain that radiated to the thigh.The principal investigator of the clinical trial assessed this as possibly related to the patient¿s breast implants.The patient was advised to do range of motion stretches to aid with muscle spasms.Patient sent to get bone scan in (b)(6) 2023.The event is still ongoing.H6 health effect clinical code e2402: generalized illness.Manufacturer¿s reference number: (b)(4).

• 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: kate karberg ; 3041 skyway circle north; irving, TX 75038 ; 3035526892
• MDR Report Key: 16072003
• Report Number: 1645337-2022-15639
• Device Sequence Number: 6262489
• Product Code: FTR
• UDI-Device Identifier: 00081317024262
• UDI-Public: 00081317024262
• 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,Health Professional
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup,Followup,Followup

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: 03/12/2025
• Device Model Number: 3341404
• Device Catalogue Number: 3341404
• Device Lot Number: 9428920
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 12/02/2022
• Supplement Date Received by Manufacturer: 04/05/2023; 05/12/2023; 08/14/2023; 10/03/2025
• Initial Report FDA Received Date: 12/29/2022
• Supplement Report FDA Received Date: 04/28/2023; 05/23/2023; 09/01/2023; 10/21/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 03/09/2020
• 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: 51 YR
• Patient Sex: Female
• Patient Weight: 58 KG
• Patient Ethnicity: Non Hispanic
• Patient Race: White