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Terminated

AEROSET Phenobarbital, LN 1E08-01

FDA Recall Z-0208-04 · Posted 2004-07-20

Recalling FirmAbbott Laboratories Diagnostic Div
Recall StatusTerminated
Product CodeLGQ
Date Initiated2003-11-03
Date Terminated2004-07-29
Product Quantity112

Reason for Recall

Assay is imprecise.

Firm Action

Firm telephoned customers on 11/3/2003 and followed up with a letter offering credit or replacement.

Root Cause

Other

Distribution Pattern

Nationwide, Mexico, England and Canada

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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