MAUDE Adverse Event Report: MENTOR TEXAS MENTOR SMOOTH ROUND HIGH PROFILE; PROSTHESIS, BREAST, INFLATABLE, INTERNAL, SALINE

Catalog Number	3503460
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Autoimmune Disorder (1732)
Date of Event	01/01/2014
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that a 37-year-old caucasian female patient underwent a primary breast augmentation with two 460cc mentor smooth round high profile saline breast prostheses and experienced autoimmune disorder symptoms including breast implant illness, fatigue, memory loss, depression, anxiety, migraines, yeast infections, anti-phospholipid syndrome, lupus, tendinitis, arthritis, hypothyroidism, pain, sleep paralysis, memory issues, brain fog, concentration issues, sleeping issues, issues with speech, unexplained bruising, hearing issues, nosebleeds, insomnia, constant fatigue, hives, rashes, mental health issues, depression, anxiety, attention deficit disorder, eating disorder, headaches, migraines, ocular migraine, carpool tunnel issues, heart burn, stomach issues, constipation, diarrhea, food sensitivity, hot flashes, clamminess, night sweats, low sex drive, issues swallowing, chocking, nausea, panic attacks, feeling like things aren¿t real, issues looking at screens, sleeping too much, tapping teeth, grinding teeth, anti-social, post nasal drip, hard to swallow, hard to clear throat, extreme weight gain, food addiction, swelling, high heart rate, breathing issues, blood clots, hormonal issues, behavioral issues, emotional issues, temperature rises, pigmentation dispersion syndrome, dry eye, allergies, mastitis, eating disorder, gestational diabetes, obsessive compulsive disorder post-operatively.At the time of this report, mentor has received no information regarding explantation or an expected explantation date.This report is for the left side device.
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: no information regarding explantation or an expected explantation date has been received.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.If certain information is unknown, not available or does not apply, the section/field of the form is left blank.Manufacturer¿s reference number: (b)(4).

• Brand Name: MENTOR SMOOTH ROUND HIGH PROFILE
• Common Device Name: PROSTHESIS, BREAST, INFLATABLE, INTERNAL, SALINE
• 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: 21428873
• Report Number: 1645337-2025-01788
• Device Sequence Number: 17294399
• Product Code: FWM
• UDI-Device Identifier: 00081317001676
• UDI-Public: (01)00081317001676(17)151031(10)6515953
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: P990075
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2012
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Other
• Type of Report: Initial

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: 10/31/2015
• Device Catalogue Number: 3503460
• Device Lot Number: 6515953
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 01/24/2025
• Initial Report FDA Received Date: 02/20/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 10/17/2011
• 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: Other
• Patient Age: 28 YR
• Patient Sex: Female
• Patient Ethnicity: Non Hispanic
• Patient Race: White