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

Medical Device Recalls

  • Print
  • Share
  • E-mail
-
91 to 100 of 275 Results
Product: pacemaker
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
Results per Page
New Searchexport reports to excelExport to Excel | HelpHelp
Product Description
Sort by Product Name [A-Z]
Sort by Product Name [Z-A]
Recall
Class
Sort by Recall Class [0-9]
Sort by Recall Class [9-0]
FDA Recall
Posting Date
Sort by Date Classified [0-9]
Sort by Date Classified [9-0]
Recalling Firm
Sort by Recalling Firm [A-Z]
Sort by Recalling Firm [Z-A]
Discovery II Multiprogrammable Pacemaker, Model 1284 2 07/15/2003 Guidant Corp-Cpi Division
Discovery II Multiprogrammable Pacemaker, Model 1283 2 07/15/2003 Guidant Corp-Cpi Division
Discovery II Multiprogrammable Pacemaker, Model 1184 2 07/15/2003 Guidant Corp-Cpi Division
Pulsar Max II Multiprogrammable Pacemaker, Model 1280 2 07/15/2003 Guidant Corp-Cpi Division
Discovery II Multiprogrammable Pacemaker, Model 0481 2 07/15/2003 Guidant Corp-Cpi Division
Pulsar Max II Multiprogrammable Pacemaker, Model 1181 2 07/15/2003 Guidant Corp-Cpi Division
Pulsar Max II Multiprogrammable Pacemaker, Model 1180 2 07/15/2003 Guidant Corp-Cpi Division
Discovery II Multiprogrammable Pacemaker, Model 0981 2 07/15/2003 Guidant Corp-Cpi Division
Discovery II Multiprogrammable Pacemaker, DDD Model 981 2 05/29/2003 Guidant Corp-Cpi Division
Discovery II Multiprogrammable Pacemaker, DDDR Model 1280 2 05/29/2003 Guidant Corp-Cpi Division
-
-