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Alkaline Phosphatase Reagent Set

CLINICAL DIAGNOSTIC SOLUTIONS, INC. · Model R1 x 500 mL, R2 x 125 mL · UDI-DI 00812137011855

CJE
10
510(k) clearances
74
Adverse events
22
Recalls
37
Facilities

Description

For the quantitative determination of alkaline phosphatase in human serum. For in vitro diagnostic use only. Serum alkaline phosphatase estimations are of interest in the diagnosis of two groups of conditions; hepatobiliary disease and bone disease associated with increased osteoblastic activity.

Recalls

DateFirmReason
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 conditions. This failur
2023-08-05Ortho-Clinical Diagnostics, INc.Samples containing high levels of ALKP (or an interfering substance) could deplete the available substrate in the reagent layer of a VITROS ALKP Slide and not post the substrate de
2013-06-12Ortho-Clinical DiagnosticsOrtho Clinical Diagnostics is recalling Slide Dispense cartridges used with some VITROS Chemistry Product Slides due to slide dispense issues.
2011-08-26Abbott Laboratories, IncThe reagent has the potential to be contaminated with mold, the Cladosporium fungal species.
2008-02-07Pointe Scientific, Inc.May be contaminated with microorganisms.
2008-02-07Pointe Scientific, Inc.May be contaminated with microorganisms.
2008-02-07Pointe Scientific, Inc.May be contaminated with microorganisms.
2008-02-07Pointe Scientific, Inc.May be contaminated with microorganisms.
2008-02-07Pointe Scientific, Inc.May be contaminated with microorganisms.
2008-02-07Pointe Scientific, Inc.May be contaminated with microorganisms.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.