Recall Z-2201-2011
Bio-Rad Laboratories · initiated July 19, 2010
Product
Software CD is labeled in part: "BLOOD VIRUS DIVISION***BIO-RAD EVOLIS System APF Version 4.4 Software Version 2.00 2009/05***" The EVOLIS Assay Protocol Files (APF) Software contains assay-specific instructions necessary for the EVOLIS Microplate processing system to process enzyme immunoassays on the EVOLIS instrument, perform data reduction and generate reports.
Codes / lots: APF Version 4.4 Software Version 2.00 2009/05 LOT=V4.4-0505-2
Reason for recall
The EVOLIS Assay Protocol Files Software is configured in such a way that may result in a miscalculation of quantitative test results and/or an error in reporting positive/negative sample values.
FDA-determined cause: Software design
Action taken
Bio-Rad Laboratories sent an Urgent Product Correction letter dated July 19, 2010, to all customer sites via FedEx. There are two issues related to The EVOLIS Assay Protocol Files (APF) Software that could potentially affect patient results. Issue 1 involves quantitative sample test/calculations/results interpretation for assays with linear regression, point to point or 4PL data reduction. Issue 2 involves sample test results with " Result Report Flags''. A software patch to correct these two issues will be sent to each customer site. Bio-Rad Laboratories will work with each customer to complete documentation confirming that the software patch has been successfully installed on each instrument. If you have any questions or concerns regarding these two issues, please contact Technical Support at 1-800-224-6723, option 2 and then option 3.
Details
- Recall number
- Z-2201-2011
- Initiated
- July 19, 2010
- Posted by FDA
- May 19, 2011
- Terminated
- August 25, 2011
- Product code
- LFX – Enzyme Linked Immunoabsorbent Assay, Rubella
- Quantity
- 272
- Distribution
- Nationwide Distribution -- Including Puerto Rico.
- Recalling firm
- Bio-Rad Laboratories, Redmond, WA