Atlas FDA

DrugCheck 3 Test Cup COC/MET/THC Product Code 60300

FDA device recall Z-1245-03 · posted 2003-09-23 · Terminated

Recall details

Recalling firm
Drug Free Enterprises Inc
Reason for recall
Label lacks professional use legend and name and address of the manufacturer.
Action taken
The firm sent a letter to customers requesting that they overlabel their stock on 3/20/2003. This recall is complete.
Root cause
Other
Status
Terminated
Product code
DIO
Quantity affected
Undetermined.
Distribution
Nationwide
Date initiated
2003-03-20
Date posted
2003-09-23
Date terminated
2003-09-22
Location
Agoura Hills, CA

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