Recall StatusTerminated
Date Initiated2020-03-02
Date Terminated2020-10-05
Product Quantity297 PCK US; 1247 PCK OUS
Reason for Recall
Negative bias for the carbohydrate-deficient transferrin (CDT) measurement in comparison to the HPLC method, observed to occur after 15 months based on shelf life monitoring
Firm Action
Siemens Healthcare Diagnostics issued Urgent Medical Device Correction (UMDC) letter PP-20-002.A.US to the 5 affected customers in the U.S. on March 5, 2020 via FedEx overnight delivery. ( Urgent Field Corrective Action (UFCA) PP20-002.A.OUS was issued to all OUS Siemens sites with affected customers electronically for distribution and regional reporting to their local competent authorities).
Letter states reason for recall, health risk, and action to take by the Customer Please review this letter with your Medical Director.
Discontinue use of and discard the kit lots listed in Table 1.
Review your inventory of these products to determine your laboratorys replacement needs and to provide information to Siemens Healthineers for reporting to the authorities. Please retain this letter with your laboratory records and forward this letter to those who may have received this product.
Contact your Siemens Healthineers Customer Care Center or your local Siemens Healthineers technical support representative.
Root Cause
Under Investigation by firm
Distribution Pattern
IN, KS, MO, OH, VA
Foreign: Australia, Austria, Bangladesh, Belgium, Canada, China
Czech Republic, Egypt, Finland, France, Germany, Great Britain, Hungary
India, Italy, Japan, Mexico, Netherlands, Norway, Poland, Portugal, Republic Korea, Russia Federation, Slovakia, Slovenia, South Africa, Spain
Sweden, Switzerland, Taiwan
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.