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U.S. Department of Health and Human Services

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

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MENTOR TEXAS MENTOR SMOOTH ROUND SPECTRUM; PROSTHESIS, BREAST, INFLATABLE, INTERNAL, SALINE Back to Search Results
Model Number 3501490
Medical Device Problem Code Material Rupture (1546)
Health Effect - Clinical Code Deformity/ Disfigurement (2360)
Date of Event 04/07/2022
Type of Reportable Event Serious Injury
Additional Manufacturer Narrative
Device evaluation summary: the product was returned to mentor for evaluation.The tubing, the connector, and the injection port were not received.Mentor conducted a visual inspection and microscopic examination of the returned device.Visual analysis of the returned sample determined that the breast implant was found to have a tear on the anterior view measuring approximately 1.2 cm.Microscopic examination was performed on the edges of the tear, and parallel striations were found in an area of the tear on the anterior view, measuring less than 0.1 cm.Parallel striations are consistent with markings made by a sharp object perforating the implant shell.The cause in the remaining area of the tear could not be identified.A manufacturing record evaluation was performed for the finished device lot number, and no non-conformances were identified.As part of mentor¿s quality process, all devices are manufactured, inspected, and released to approved specifications.Additional complaint information monitoring for potential safety signals is conducted through complaint trending as part of post-market surveillance.Reason for device explant and/or reoperation: deflation.Manufacturer¿s reference number: (b)(4).
 
Event or Problem Description
It was reported that a 70-year-old caucasian female who had a mentor smooth round spectrum 575cc saline prostheses placed experienced bilateral deflation post procedure.The deflation was diagnosed in the physician¿s office.As a result, explant was performed on (b)(6) 2022.The right sided deflation was reported initially under 1645337-2022-05896 on may 19, 2022.On may 27, 2022 mentor became aware that the returned left sided device also appeared to have been deflated.This report relates to the left prosthesis.
 
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Brand Name
MENTOR SMOOTH ROUND SPECTRUM
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
michelleann garcia
3041 skyway circle north
irving, TX 75038
646591-7981
MDR Report Key14658723
Report Number1645337-2022-06849
Device Sequence Number3739804
Product Code FWM
UDI-Device Identifier00081317002048
UDI-Public00081317002048
Combination Product (Y/N)N
Initial Reporter StateNY
Initial Reporter CountryUS
PMA/510(K) Number
P990075
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2004
Device Explanted Year2022
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Health Professional
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? Yes
Operator of Device Health Professional
Device Expiration Date06/30/2007
Device Model Number3501490
Device Catalogue Number3501490
Device Lot Number263184
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer05/24/2022
Type of Report(Section G)Initial
Initial Date Received by Manufacturer 05/27/2022
Initial Report FDA Received Date06/10/2022
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured06/01/2003
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 Number1
Outcome Attributed to Adverse Event Required Intervention;
Patient Age70 YR
Patient SexFemale
Patient EthnicityNon Hispanic
Patient RaceWhite
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