Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 76991

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
November 29, 2014
Product types
Device
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Magellan Diagnostics, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

Magellan Diagnostics LeadCare Ultra Blood Analyzer Part Number: 80-0010

Z-1925-2017
Recall number
Z-1925-2017
Initiated
November 29, 2014
Classification
Class I
Status
Terminated
Quantity
49 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate falsely low lead concentrations in some blood samples. The issue is observed when blood samples are collected in tubes with lavender and tan rubber stoppers of the Becton Dickinson EDTA Vacutainer tubes, a collection device used with the testing system.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate falsely low lead concentrations in some blood samples. The issue is observed when blood samples are collected in tubes with lavender and tan rubber stoppers of the Becton Dickinson EDTA Vacutainer tubes, a collection device used with the testing system.

Code information

All serial numbers

Distribution pattern

Nationwide Distribution

device · product 2 of 2

Magellan Diagnostics LeadCare Ultra Blood Lead Test Kits Part Number: 80-0010

Z-1926-2017
Recall number
Z-1926-2017
Initiated
November 29, 2014
Classification
Class I
Status
Terminated
Quantity
1016

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate falsely low lead concentrations in some blood samples. The issue is observed when blood samples are collected in tubes with lavender and tan rubber stoppers of the Becton Dickinson EDTA Vacutainer tubes, a collection device used with the testing system.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate falsely low lead concentrations in some blood samples. The issue is observed when blood samples are collected in tubes with lavender and tan rubber stoppers of the Becton Dickinson EDTA Vacutainer tubes, a collection device used with the testing system.

Code information

Kit lots: 1309BU,1310AU,1312BU,1404AU,1408BU

Distribution pattern

Nationwide Distribution