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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MENTOR SMOOTH ROUND MOD PLUS PROFILE - SALINE; BREAST IMPLANTS

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MENTOR SMOOTH ROUND MOD PLUS PROFILE - SALINE; BREAST IMPLANTS Back to Search Results
Model Number 350-2450
Health Effect - Clinical Codes Fatigue (1849); Pain (1994); Thyroid Problems (2102); Arthralgia (2355); Palpitations (2467)
Date of Event 01/01/2016
Type of Reportable Event Serious Injury
Event or Problem Description
Adrenal fatigue, hypothyroidism, hashimotos, back and shoulder pain on left side, lower back pain - left side, heart palpitations.
 
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Brand Name
SMOOTH ROUND MOD PLUS PROFILE - SALINE
Common Device Name
BREAST IMPLANTS
Manufacturer (Section D)
MENTOR
MDR Report Key6669671
Report NumberMW5070658
Device Sequence Number10563464
Product Code FWM
Initial Reporter StateTX
Initial Reporter CountryUS
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2012
Reporter Type Voluntary
Initial Reporter Occupation Patient
Type of Report Initial
Report Date (Section B) 06/24/2017
2 Devices were Involved in the Event: 1   2  
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Operator of Device No Information
Device Model Number350-2450
Device Lot Number6404302
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date06/24/2017
Patient Sequence Number1
Outcome Attributed to Adverse Event Required Intervention;
Patient Age40 YR
Patient Weight66
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