Atlas FDA

Clinical Chemistry Urea Nitrogen

FDA device recall Z-0550-04 · posted 2004-02-26 · Terminated

Recall details

Recalling firm
Abbott Laboratories Diagnostic Div
Reason for recall
Low results due to contaminant.
Action taken
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
Status
Terminated
Quantity affected
568
Distribution
Nationwide, Mexico, Argentina, Germany, Australia, Venezuela, Puerto Rico, Singapore, New Zealand, Columbia, Canada, Hong Kong, Grand Cayman
Date initiated
2003-11-24
Date posted
2004-02-26
Date terminated
2012-02-07
Location
South Pasadena, CA

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