Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MDR Database Search
  • 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
 

New Search Back To Search Results
BRAND NAMESURGICAL MESH
MANUFACTURER
VASCULAR SYSTEM DIV., C.R. BARD., INC.
129 CONCORD RD
BELLERICA MA 01821
ACCESS NUMBERM544127
PRODUCT CODEFTM
PANELGENERAL AND PLASTIC SURGERY
REPORT TYPESERIOUS INJURY
DATE FDA RECEIVED08/04/1994
EVENT DESCRIPTION TYPEPRELIMINARY
EVENT DESCRIPTION
THE PT EXPERIENCED A SEVERE REACTION AFTER THE DEVICE WAS IMPLANTED, RESULTING IN PHYSICAL PAIN. PRODUCT WAS IMPLANTED ON 12/4/91. THE CAUSE FOR PAIN WAS DISCOVERED IN 4/94.
-
-