Recalls from Siemens Healthcare Diagnostics, Inc.

• Atellica CH Revised C-Reactive Protein (RCRP) (opens in a new tab)
  Moderate risk, FDA, Oct 1, 2026, Device defect
• Siemens Healthcare Diagnostics Beckman Coulter and Syva EMIT 2000 Quinidine Assay (opens in a new tab)
  Moderate risk, FDA, Aug 17, 2026, Device defect
• Siemens Healthcare Diagnostics Atellica CH Urine Albumin (opens in a new tab)
  Moderate risk, FDA, Aug 5, 2026, Device defect
• Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls (opens in a new tab)
  Low risk, FDA, Aug 4, 2026, Quality testing problem
• Syva Emit Disopyramide Assay Enzyme Immunoassay (opens in a new tab)
  Low risk, FDA, Aug 4, 2026, Quality testing problem

Data: Recall Canary (opens in a new tab)