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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 No Code Available (3191)
Date of Event 01/01/2020
Type of Reportable Event Serious Injury
Additional Manufacturer Narrative
Since the device has not been returned for analysis, 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 is in progress.Once completed, a supplemental report will be submitted.Reason for device explant and/or reoperation: deflation.Manufacturer¿s reference number: (b)(4).
 
Event or Problem Description
It was reported that a (b)(6) year-old female patient underwent a primary breast augmentation with a 575cc mentor smooth round spectrum prosthesis and experienced postoperative right-sided deflation.The patient went in for a consultation on (b)(6) 2020, and the diagnosis was confirmed by a healthcare professional.As a result, the patient underwent removal and replacement with an unspecified saline implant on (b)(6) 2020.
 
Additional Manufacturer Narrative
On 23-mar-2020, the mentor failure analysis lab has received the device for evaluation.The analysis has begun but is not complete at this time.When the investigational analysis has been completed, a supplemental report will be submitted.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.Manufacturer's reference number: (b)(4).
 
Additional Manufacturer Narrative
On 16-apr-2020, the investigation on the suspected medical device was completed.Investigation summary : during visual evaluation of the sample, no apparent damage was observed.Leak testing was performed, in accordance with mentor procedures, and no leak sites were detected.After a thorough analysis, mentor was unable to confirm the reported issue.Each device is visually inspected during manufacturing to ensure the device meets the required specifications prior to shipment.Manufacturer's reference number: (b)(4).
 
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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
MDR Report Key9862363
Report Number1645337-2020-04537
Device Sequence Number16797137
Product Code FWM
UDI-Device Identifier00081317002048
UDI-Public00081317002048
Combination Product (Y/N)N
Initial Reporter StateCA
Initial Reporter CountryUS
PMA/510(K) Number
P990075
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2007
Device Explanted Year2020
Reporter Type Manufacturer
Report Source health professional
Initial Reporter Occupation Other
Type of Report Initial,Followup,Followup
Report Date (Section B) 02/25/2020
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 Date09/27/2010
Device Model Number3501490
Device Catalogue Number3501490
Device Lot Number5706028
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer03/23/2020
Initial Date Received by Manufacturer 02/25/2020
Supplement Date Received by Manufacturer03/23/2020
04/16/2020
Initial Report FDA Received Date03/20/2020
Supplement Report FDA Received Date04/09/2020
04/17/2020
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
Outcome Attributed to Adverse Event Required Intervention;
Patient Age61 YR
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