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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