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

Medical Device Recalls
  • Print
  • Share
  • E-mail
-
1 to 5 of 5 Results
510(K) Number: K161359
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]
MyLab Alpha, Model 7400 2 10/23/2018 FEI # 3012981490
ESAOTE S.P.A.
MyLab Gamma, Model 7410 2 10/23/2018 FEI # 3012981490
ESAOTE S.P.A.
MyLab Seven, Model 6400 2 10/23/2018 FEI # 3012981490
ESAOTE S.P.A.
AC/DC POWER SUPPLY for 7400, Part Number 151004300, XP Power Model Number AHM180PS19-XE0338, AC/DC A... 2 09/30/2020 FEI # 3014563045
ESAOTE S.P.A
AC/DC POWER SUPPLY for 7400, Part Number 151004301, XP Power Model Number AHM180PS19-XE1057, AC/DC A... 2 09/30/2020 FEI # 3014563045
ESAOTE S.P.A
-
-