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Recall Observatory FDA recall evidence

Device product

Magellan LeadCare¿ II Blood Lead Test Kit. In Vitro Test for the measurement of lead in fresh whole blood. Catalog Number: 70-6762 Primary DI No: 00850355006000 The LeadCare II Blood Lead Test Kit is for in vitro diagnostic use only. The test kit is for the quantitative measurement of lead in fresh whole blood. This product is for professional use only. Sensors and treatment reagent of the test kit are specific for lead only. Contents of the LeadCare II Blood Lead Test Kit must only be used with a LeadCare II Analyzer.

Z-0285-2019

August 08, 2018

Class II

Product summary

Firm
Magellan Diagnostics, Inc.
Event
Event 81074
Status
Terminated
Classification
Class II
Quantity
1,465 kits
Official record key
device-enforcement:Z-0285-2019

Official wording

Reason: Defect with the calibration button for lot 1808M. Level 1 and Level 2 Quality Control (QC) values will generate results of HIGH (>65 ¿g/dL). Results for patient testing with this lot will be displayed as HIGH.

Code information: Lot 1808M and sub-lots: 1808M-01, 1808M-02, 1808M-03, 1808M-04, 1808M-05, 1808M-06, 1808M-07, 1808M-08, 1808M-09. Exp. Date:November 10, 2019

Distribution pattern: Worldwide distribution: US (Nationwide) and countries of: Spain and South Africa.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Defect with the calibration button for lot 1808M. Level 1 and Level 2 Quality Control (QC) values will generate results of HIGH (>65 ¿g/dL). Results for patient testing with this lot will be displayed as HIGH.