• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services


  • Print
  • Share
  • E-mail
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC

ETHICON PHYSIOMESH Back to Search Results
Catalog Number PHY2025V
Device Problem Insufficient Information (3190)
Patient Problem Unspecified Infection (1930)
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.

Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Type of DeviceMESH
Manufacturer (Section D)
3348 pulliam st.
san angelo TX 76905
MDR Report Key2363232
MDR Text Key2509148
Report Number2363232
Device Sequence Number1
Product Code FTL
Combination Product (Y/N)
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
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