• 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: K140522
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]
Immunoassay Premium Level 3-In vitro diagnostic use, as assayed quality control material to monitor ... 3 06/28/2023 Randox Laboratories Ltd.
Immunoassay Premium Control Tri Level-In vitro diagnostic use, as assayed quality control material t... 3 06/28/2023 Randox Laboratories Ltd.
Immunoassay Premium Plus Controls, Model Numbers IA3109 and IA3112 Product Usage: This product i... 3 04/08/2019 Randox Laboratories Ltd.
Immunoassay Premium Controls (3x4x5mL and 12x5mL packages) 3 03/12/2018 Randox Laboratories
Immunoassay Premium Plus Controls (3x4x5mL and 12x5mL packages) 3 03/12/2018 Randox Laboratories
-
-