Bio-Rad brand Meridian ANA Screen ELISA Test Kit, 96 Test, Catalog No. 4884261, Manufactured by: Bio-Rad Laboratories, Inc. Hercules, CA and distributed by Meridian Diagnostics.
FDA Recall Z-0613-2011 · Posted 2010-12-13
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Recalling FirmBio-Rad Laboratories Inc
Recall StatusTerminated
Product CodeLKJ
Date Initiated2010-02-24
Date Terminated2011-01-10
Reason for Recall
False positive test results caused by decrease in the OD values of ANA Cutoff Controls and ANA Positive Controls. The increased positivity rates were associated with the Meridian ANA Screening kit. False positive ANA values could result in misdiagnosis or mistreatment .
Firm Action
Bio-Rad issued an Urgent Medical Device Recall NOtification letter dated February 24, 2010 to their distributor, identifying the affected product and actions to be taken. The distributor was instructed to examine inventory and quarantive affected kit lots, and to identify and notify customers with affected lots to discontinue use and discard the product. Replacement kits will be distributed. Customers were asked to complete and return a recall response form.
Bio-Rad can be contacted at 510 724-7000 concerning this recall.
Root Cause
Other
Distribution Pattern
Nationwide Distribution: to Meridian Diagnostics in Ohio.
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.
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