Clinical Chemistry Urea Nitrogen
FDA Recall Z-0550-04 · Posted 2004-02-26
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Recalling FirmAbbott Laboratories Diagnostic Div
Recall StatusTerminated
Date Initiated2003-11-24
Date Terminated2012-02-07
Product Quantity568
Reason for Recall
Low results due to contaminant.
Firm Action
Each domestic customer will receive the recall letter by direct mailing. Foreign affiliates will be responsible for distributing letters to thier customers. Letters were sent 11/24/2003. A reply form was enclosed.
Root Cause
Other
Distribution Pattern
Nationwide, Mexico, Argentina, Germany, Australia, Venezuela, Puerto Rico, Singapore, New Zealand, Columbia, Canada, Hong Kong, Grand Cayman
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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