Sentinel Ch Spa recalls

Sentinel Ch Spa appears in 8 official U.S. recall notices indexed by RecallRadar, most recently on 2023-11-29.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Alinity c Iron Reagent, Reference Number 08P3920
  FDA Device · Class II · 2023-11-29 · Sentinel Ch Spa
• IRON assay, Reference Numbers 6K95-41 and 6K95-30
  FDA Device · Class II · 2023-11-29 · Sentinel Ch Spa
• Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit (ref 07P5605) - Product Usage: use in the calibration of the Alinity c CRP Vari…
  FDA Device · Class III · 2021-10-13 · Sentinel Ch Spa
• ACE Control Set - IVD Control set for the quantitative determination of Angiotensin Converting Enzyme (ACE) REF 1667001
  FDA Device · Class III · 2021-07-14 · Sentinel Ch Spa
• MULTIGENT Lithium-intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c…
  FDA Device · Class II · 2019-10-02 · Sentinel Ch Spa
• Alinity c Lithium Reagent Kit- intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and t…
  FDA Device · Class II · 2019-10-02 · Sentinel Ch Spa
• MULTIGENT Creatinine (Enzymatic), Catalog Numbers 8L24-31 and 8L24-41
  FDA Device · Class II · 2017-08-09 · Sentinel Ch Spa
• Sentinel MULTIGENT Ammonia Ultra Reagent, In-Vitro Diagnostic for ammonia measurement
  FDA Device · Class II · 2015-11-04 · Sentinel Ch Spa