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 6 of 6 Results
510(K) Number: K053153
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]
Clinical Chemistry Calibration Serum (Catalog number Cal2351) that is 20x5ml lyophilized human based... 2 05/03/2024 FEI # 1000361607
Randox Laboratories Ltd.
Calibration Serum Level 3. CAL 3, REF CAL2351. Human Assayed Multi-Sera Level 2 (HN1530) Human Assay... 2 01/18/2024 FEI # 1000361607
Randox Laboratories Ltd.
Calibration Serum Level 3 - IVD For use as a Calibrator in clinical chemistry assays Catalog Number... 2 01/18/2024 FEI # 1000361607
Randox Laboratories Ltd.
Calibration Serum Level 3 CAL2351 2 01/18/2024 FEI # 1000361607
Randox Laboratories Ltd.
Calibration Serum Level 3 (CAL 3) - multi-analyte mixture calibrator. Catalogue Number: CAL2351 2 05/12/2021 FEI # 8020890
Randox Laboratories Ltd.
This is an in vitro diagnostic product intended for use as a calibration serum in clinical chemistry... 3 09/07/2019 FEI # 1000361607
Randox Laboratories Ltd.
-
-