Recall StatusTerminated
Date Initiated2017-04-27
Date Terminated2017-08-14
Product Quantity198 kits
Reason for Recall
According to Randox Laboratories an investigation indicates a labelling error for 2 of the test methods listed for quantification of Total Protein (urine). The values for the mean of all instruments are incorrect by a factor of 10. Instrument specific values are correct. This does not affect the performance or stability claims of the product.
As control results will be outside of the quoted range this may result in a delay in reporting the sample test results.
However as the correct instrument specific means are also included in the value sheet this delay is unlikely. Customers have been referred to their Medical Director for further advice
Firm Action
Randox Laboratories will contact Customers directly by e-mail and will be followed up with once every 2 weeks over a period of 6 weeks. There are no plans in place to follow up with customers after the 6 week period. For further questions, please call (304) 728-2890.
Root Cause
Error in labeling
Distribution Pattern
Worldwide Distribution - US Distribution to Puerto Rico and to the countries of :
Canada
Kuwait
Chile
Poland
China
Romania
France
Saudi Arabia
Guatemala
Slovenia
Iran
UAE
India
UK
Italy
Uruguay
Iraq
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.