• 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
-
1 to 10 of 17 Results
510(K) Number: K193056
 
 1 
 2 
 > 
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]
Puritan Bennett 980 Series Ventilator 1 04/25/2022 Covidien, LP
Puritan Bennett 980 Series Ventilator, 980S1ENDICU 1 12/09/2021 Covidien, LP
Puritan Bennett 980 Series Ventilator, 980S3ENDICU 1 12/09/2021 Covidien, LP
Puritan Bennett 980 Series Ventilator, 980U1ENASAA 1 12/09/2021 Covidien, LP
Puritan Bennett 980 Series Ventilator, 980U1ESDIUC 1 12/09/2021 Covidien, LP
Puritan Bennett 980 Series Ventilator, 980U3ESDIUU 1 12/09/2021 Covidien, LP
Puritan Bennett 980 Series Ventilator,980X1ENAIQC 1 12/09/2021 Covidien, LP
Puritan Bennett 980 Series Ventilator, 980X1ENDIPC 1 12/09/2021 Covidien, LP
Puritan Bennett 980 Series Ventilator, 980X1ENDIUU 1 12/09/2021 Covidien, LP
Puritan Bennett 980 Series Ventilator, 980X1ENNISB 1 12/09/2021 Covidien, LP
-
-