Reported Apr 29, 2026 · Ongoing

(1)(2) LeadCare¿ II Blood Lead Test Kit, (3)LeadCare¿ II 5X Blood Lead Test Kit, (4)LeadCare¿ II 9X Blood Lead Test Kit…

Magellan Diagnostics, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Magellan Diagnostics, Inc. · 101 Billerica Ave Bldg 4 · North Billerica, MA · 01862-1271

Is this the product you have?

    • (1)(2) LeadCare¿ II Blood Lead Test Kit
    • (3)LeadCare¿ II 5X Blood Lead Test Kit
    • (4)LeadCare¿ II 9X Blood Lead Test Kit
  • Catalog Number(s)
    • (1) 70-6762
    • (2) 70-6762RUO
    • (3) 70-8404 (Box containing 5 Test Kits)
    • (4) 70-9000 (Box containing 9 test kits)
    • The LeadCare II kit is
  • provided with the following materials" Sensors (2 Containers of 24 sensors each; 48 tests) " Treatment Reagent Tubes (2 packages of 24 tubes each; 48 tests) " Heparinized Capillary Tubes/Plungers (50 @) " Transfer Droppers (50 @) " Calibration Button (1 @) " Lead Control Level 1 (1 @ 2 mL) " Lead Control Level 2 (1 @ 2 mL)
Lot codes and dates

9 of 9 products

Products covered by this recall
#BarcodesProduct as published
1Catalog Number(s): (1) 70-6762, (2) 70-6762RUO
200850355006000UDI-DI: 00850355006000
3ALL lots and ALL sublots
4Catalog Number(s): (3) 70-8404
500850355006086UDI-DI: 00850355006086
6ALL lots and ALL sublots
7Catalog Number(s): (4) 70-9000
800850355006093UDI-DI: 00850355006093
9ALL lots and ALL sublots
Amount recalled
197893

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide
  • GA

Why it was recalled

Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing with the LeadCare Test Systems. False positive lead results may cause delayed results and additional unnecessary testing.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:16 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.