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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CONVATEC INC. S4S/SUR-FIT NATURA 2 PC - 2 PC STOMAHESIVE (SH; PROTECTION OSTOMY

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CONVATEC INC. S4S/SUR-FIT NATURA 2 PC - 2 PC STOMAHESIVE (SH; PROTECTION OSTOMY Back to Search Results
Model Number 125259
Device Problem Human-Device Interface Problem (2949)
Patient Problems Inflammation (1932); Itching Sensation (1943); Rash (2033)
Event Type  Injury  
Event Description
Report provided by the end user indicated the development of an itchy, inflamed rash under peristoma skin mass which increasingly became worse over time.The end user subsequent outcome was not reported.
 
Manufacturer Narrative
Analysis is taken from a trending report of evaluations or adverse events finalized (b)(6) 2011.The data presented is from three different product applications.The report states that there are no significant trends.
 
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Brand Name
S4S/SUR-FIT NATURA 2 PC - 2 PC STOMAHESIVE (SH
Type of Device
PROTECTION OSTOMY
Manufacturer (Section D)
CONVATEC INC.
211 american ave.
greensboro NC 27409
Manufacturer Contact
matthew walenciak, director post
211 american ave.
greensboro, NC 27409
9083779293
MDR Report Key4132836
MDR Text Key4791913
Report Number1049092-2014-11747
Device Sequence Number1
Product Code EXE
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K830945
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Consumer,Company Representative
Reporter Occupation Not Applicable
Type of Report Initial
Report Date 06/17/2013
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received09/29/2014
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Lay User/Patient
Device Model Number125259
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received06/17/2013
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Weight82
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