Magellan Diagnostics expanded the Class I recall of its LeadCare II Blood Lead Test Kits, LeadCare Plus Blood Lead Test Kits and LeadCare Ultra Blood Lead Test Kits for the detection of lead in whole blood. 

Magellan Diagnostics received reports that control tests of either the “Low-Control” (e.g., the “Level 1” control at approximately 9 g/dL ± 3g/dL) and/or the “High-Control” (e.g., the “Level 2” control at approximately 28 g/dL ± 4g/dL) generated a “low” result (i.e., “Control Out of Range-Low” [“COOR-L”]). Magellan initiated the recall because the impacted LeadCare Test Kits lots could potentially underestimate blood lead levels when processing patient blood samples.

Magellan Diagnostics Recall Background

In May 2021, Magellan Diagnostics initiated this voluntary recall after identifying an ongoing issue with testing of the controls included in the LeadCare Test Kits. Magellan provides two controls in the test kits, which are designed to mimic blood and are spiked with lead to specific target values with an associated acceptable range. Results of the control tests within the acceptable range indicate that the system is operating properly before testing patient samples

  • Health Care Providers should evaluate patient test results that were generated with all recalled lots. 
    1. Suspect results should be confirmed with an alternative lead testing option, such as those using Inductively Coupled Plasma Mass Spectrometry (ICP-MS) or Graphite Furnace Atomic Absorption Spectroscopy (GFAAS) at a high complexity, CLIA-certified, reference laboratory.
    2. See CDC’s recommended actions based on blood lead level:
  • Customers should discontinue use of all Magellan Diagnostics LeadCare Test Kits’ lots identified as part of the recall and quarantine remaining inventory.

Health professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program:

  • Complete and submit the report online.
  • Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on form, or submit by fax to 1-800-FDA-0178.