Recall StatusTerminated
Date Initiated2016-08-08
Date Terminated2018-10-03
Product Quantity2,248 kits
Reason for Recall
Failure of analytical sensitivity with Calibrator U kit lots ending in 63 and 64 and a drift from the internal standardization
Firm Action
Siemens Healthcare Diagnostics issued an Urgent Medical Device Correction (UMDC) to customers in the US on August 8, 2016, to be delivered to customers on August 9, 2016.
An Urgent Field Safety Notice (UFSN) was sent out for distribution to all customers outside the United States on August 8, 2016. The communications notify customers of the failure of analytical sensitivity with Calibrator U kit lots ending in 63 and 64 and a drift from the internal standardization. The communications also inform customers that analytical sensitivity and alignment to the internal standardization will be restored with the release of Calibrator U kit lots ending in 65.
Customers may continue to use Calibrator U lots CU63 and CU64 with any indate reagent kit lot, current QC ranges and current Master Curve Material lot 45719. Revised QC targets and ranges are located on the Bio-Rad website at QCnet.com for use with CU65 and higher. For further questions, please call (508) 668-5000.
Root Cause
Nonconforming Material/Component
Distribution Pattern
Worldwide Distribution - Nationwide Distribution including the countries of:
Argentina
Australia
Brazil
Canada
Chile
China
Ecuador
India
Japan
Korea
Mexico
Malaysia
Peru
Philippines
Saudi Arabia
Singapore
Taiwan
Vietnam
South Africa
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.