AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part Number (REF): 5024501 3200MD series and 4500MD series are mass spectrometers intended to identify inorganic or organic compounds (e.g., lead, mercury, and drugs) in human specimens by ionizing the compound under investigation and separating the resulting ions by means of an electrical and magnetic field according to their mass. It is intended for in vitro diagnostic purposes. For in vitro diagnostic use.
FDA Recall Z-2526-2016 · Posted 2016-08-12
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Recalling FirmAb Sciex
Recall StatusTerminated
Product CodeDOP
Date Initiated2016-06-16
Date Terminated2017-03-02
Product Quantity124 units
Reason for Recall
MultiQuant MD software where under certain conditions a user
can be presented with incorrect quantitative results when using the Sum Multiple Ions feature.
Firm Action
AB SCIEX issued recall notification by letter dated June 16, 2016, to all affected customers. The letter identified the problem, provided temporary measures until a permanent software is available. A response form was to be completed and returned. questions regarding this notice
contact SCI EX at +1 289 982 2712.
Root Cause
Software design
Distribution Pattern
Worldwide Distribution - US (Nationwide) Internationally to Canada, Austria, China, Netherlands, Norway, India, Korea, Germany, France, Switzerland, Ireland, Italy, Singapore, Russia, UK, Malaysia,
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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