Sentinel CH SpA recalls

8 recalls on record · latest: September 29, 2023

Official U.S. recall history for Sentinel CH SpA, compiled from official government records.

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Sentinel CH SpA recalls IRON assay, Reference Numbers 6K95-41 and 6K95-30

September 29, 2023 · Medical device recalls Moderate risk A high recovery of Iron assay has been observed at some customer sites. Interna…

Sentinel CH SpA recalls Alinity c Iron Reagent, Reference Number 08P3920

September 29, 2023 · Medical device recalls Moderate risk A high recovery of Iron assay has been observed at some customer sites. Interna…

Sentinel CH SpA recalls Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit (ref 07P5605) - Product Usage: use in the calibration of th…

July 29, 2021 · Medical device recalls Calibrator vials were incorrectly labeled. Use of incorrectly labeled vials wil…

Sentinel CH SpA recalls ACE Control Set - IVD Control set for the quantitative determination of Angiotensin Converting Enzyme (ACE) REF 1667001

April 30, 2021 · Medical device recalls Claim for stability after reconstitution from lyophilized to liquid form does n…

Sentinel CH SpA recalls MULTIGENT Lithium-intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c System…

June 28, 2019 · Medical device recalls Moderate risk Added an additional SmartWash parameter for the Lithium and Alinity c Lithium R…

Sentinel CH SpA recalls Alinity c Lithium Reagent Kit- intended for the quantitation of lithium in serum or plasma using respectively the ARCHI…

June 28, 2019 · Medical device recalls Moderate risk Added an additional SmartWash parameter for the Lithium and Alinity c Lithium R…

Sentinel CH SPA recalls MULTIGENT Creatinine (Enzymatic), Catalog Numbers 8L24-31 and 8L24-41; IVD. Intended for the quantitative determination…

May 22, 2017 · Medical device recalls Moderate risk Reagent 1 component may result in Quality Control values shifting out of accept…

Sentinel CH SpA recalls Sentinel MULTIGENT Ammonia Ultra Reagent, In-Vitro Diagnostic for ammonia measurement; List Number: LN 6K89-30. Intende…

September 22, 2015 · Medical device recalls Moderate risk Results for ammonia are below the linear range of the assay for samples that ha…