Abbott Laboratories Diagnostic Div AEROSET Phenobarbital, LN 1E08-01 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AEROSET Phenobarbital, LN 1E08-01
Brand
Abbott Laboratories Diagnostic Div
Lot Codes / Batch Numbers
Lots: 01066HW00 expires 10/31/2003 06030HW00 expires 4/30/2004 08060HW00 expires 7/31/2004
Products Sold
Lots: 01066HW00 expires 10/31/2003 06030HW00 expires 4/30/2004 08060HW00 expires 7/31/2004
Abbott Laboratories Diagnostic Div is recalling AEROSET Phenobarbital, LN 1E08-01 due to Assay is imprecise.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Assay is imprecise.
Recommended Action
Per FDA guidance
Firm telephoned customers on 11/3/2003 and followed up with a letter offering credit or replacement.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026