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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ETHICON PHYSIOMESH

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ETHICON PHYSIOMESH Back to Search Results
Catalog Number PHY2025V
Event Date 11/11/2011
Event Type  No Answer Provided  
Event Description

Patient had mesh implanted. Patient returned to surgery 13 days later because mesh was infected.

 
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Brand NamePHYSIOMESH
Type of DeviceMESH
Manufacturer (Section D)
ETHICON
3348 pulliam st.
san angelo TX 76905
MDR Report Key2363232
Report Number2363232
Device Sequence Number1
Product CodeFTL
Report Source User Facility
Reporter Occupation
Type of Report Initial
Report Date 11/30/2011
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received11/30/2011
Is This An Adverse Event Report? No
Is This A Product Problem Report? No
Device Operator INVALID DATA
Device Catalogue NumberPHY2025V
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? Yes
Was the Report Sent to FDA? Yes
Date Report Sent to FDA11/30/2011
Event Location Hospital

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