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Terminated

DrugCheck 8 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP Product Code 60800

FDA Recall Z-1253-03 · Posted 2003-09-23

Recalling FirmDrug Free Enterprises Inc
Recall StatusTerminated
Product CodeDIO
Date Initiated2003-03-20
Date Terminated2003-09-22
Product QuantityUndetermined.

Reason for Recall

Label lacks professional use legend and name and address of the manufacturer.

Firm Action

The firm sent a letter to customers requesting that they overlabel their stock on 3/20/2003. This recall is complete.

Root Cause

Other

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

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

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