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Phosphomolybdate (Colorimetric), Inorganic Phosphorus

FDA product code CEO · Class 1 · Clinical Chemistry

89
Registered devices
113
Adverse events
8
Recalls
105
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-09-03Beckman Coulter Inc.Specific SYNCHRON Systems Modular Chemistry Phosphorus (PHOSm REF 467868) reagent lots may fail calibration before the lot expiration date which causes a delay
2025-04-24Mckesson Medical-Surgical Inc. Corporate Officetransit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage con
2013-08-12Abbott Laboratories, IncReagent lots 64736UN12, 03991UN13, 51611UN13, 74805UN12, and 03992UN13 have incorrect expiration dates assigned by Supplier.
2013-06-12Ortho-Clinical DiagnosticsOrtho Clinical Diagnostics is recalling Slide Dispense cartridges used with some VITROS Chemistry Product Slides due to slide dispense issues.
2013-02-22Siemens Healthcare Diagnostics, Inc.Siemens Healthcare Diagnostics has initiated a voluntary field action for Dimension(R) PHOS Flex(R) Reagent due to reagent interaction causing falsely depressed
2012-10-10Alfa Wassermann, Inc.Inorganic phosphorus assays using System Diluent Lot 155599 may not product acceptable calibration results.
2010-05-04Abbott Laboratories Inc.Product may give inaccurate results and aspiration errors with reagent configuration, including results outside of linear range & calibration failure.
2007-01-30Abbott Laboratories Inc.Patient results are falsely decreased by up to 15% at these levels: 1) Serum Plasma phosphorus greater than 8.0 mg/dL (2.60 mmol/L) 2) Urine phosphorus greater

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