RecallDepth

ARCHITECT HAVAB-M Assay Reagent; a chemiluminescent microparticle immunoassay (CMIA) for the qualitative detection of IgM antibody to hepatitis A virus (IgM anti-HAV) in human adult and pediatric serum and plasma (dipotassium EDTA, lithium heparin, and sodium heparin) and neonatal serum; Distributed by Abbott Laboratories, Abbott Park, IL 60064 USA, List 6L21-25

Company
Abbott Laboratories
Recall Initiated
April 20, 2011
Posted
June 6, 2011
Terminated
February 10, 2012
Recall Number
Z-2413-2011
Quantity
788 kits
Firm Location
Abbott Park, IL

Reason for Recall

The HAVAB-M reagent lot has reduced specificity and may cause an increase in false grayzone and/or false reactive results.

Distribution

Nationwide Distribution including Puerto Rico

Lot / Code Info

List 6L21-25, lot 93794HN00, expiration date 2011-09-15

Root Cause

Nonconforming Material/Component

Action Taken

Abbott Laboratories issued a Product Recall letters dated April 20, 2011 to all affected customers that received ARCHITECT HAVAB-M reagent, lot 93794HN00. The letters informed the accounts of the increased grayzone and/or reactive results and were instructed to discontinue use of the lot and destroy any remaining inventory of the lot according to laboratory procedures. If the account did not have an alternate lot of reagent, they were told to continue using the recalled lot until their lab receives the replacement lot, and to perform supplemental testing with another HAVAB-M method to confirm the results for all specimens that are grayzone or reactive. The accounts were also requested to complete and fax back to Abbott the enclosed customer reply sheet, acknowledging the receipt and understanding of the recall. For further questions regarding this please contact Abbott at 1-877-422-688

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