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Recall Observatory FDA recall evidence

Device product

Consult Diagnostics¿ Eon Calcium Reagent For In-Vitro Diagnostic Use PN: 1429 For the quantitative measurement of calcium in plasma and serum

Z-0733-2014

August 29, 2013

Class II

Product summary

Firm
Vital Diagnostics, Inc.
Event
Event 66202
Status
Terminated
Classification
Class II
Quantity
213 units
Official record key
device-enforcement:Z-0733-2014

Official wording

Reason: High positive calcium bias on plasma sample versus results on serum

Code information: All lots

Distribution pattern: Nationwide Distribution

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    High positive calcium bias on plasma sample versus results on serum