AEROSET Phenobarbital, LN 1E08-01
FDA device recall Z-0208-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Abbott Laboratories Diagnostic Div
- Reason for recall
- Assay is imprecise.
- Action taken
- Firm telephoned customers on 11/3/2003 and followed up with a letter offering credit or replacement.
- Root cause
- Other
- Status
- Terminated
- Product code
- LGQ
- Quantity affected
- 112
- Distribution
- Nationwide, Mexico, England and Canada
- Date initiated
- 2003-11-03
- Date posted
- 2004-07-20
- Date terminated
- 2004-07-29
- Location
- South Pasadena, CA
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