FDAMay 7, 2021device

LeadCare Ultra Blood Lead Test Kit Catalog Number 70-8098

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Magellan has received reports that control tests of either the Low-Control and/or the High-Control generated a low result. The issue may cause the underestimation of blood lead levels in patient samples.

What to do

FDA enforcement status: Terminated

Brands named

magellan diagnosticsmagellan

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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LeadCare Ultra Blood Lead Test Kit Catalog Number 70-8098 — Recall Details · AllClear