According to a report of Siemens Healthcare Diagnostics Inc., due to discrepancy in the testing results of particular batches of High Sensitivity C Reactive Protein Calibrator (hsCRP CAL) which cannot be identified in quality control, the manufacturer initiated the voluntary recall of the product. The recall is identified as a Class III recall. For details on product models, specifications and batches, see the Report Form of Medical Device Recall.

Attachment: Report Form of Medical Device Recall

 December 11，2019