Drug Free Enterprises Inc DrugCheck 8 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP Product Code 60800 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DrugCheck 8 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP Product Code 60800
Brand
Drug Free Enterprises Inc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
All
Drug Free Enterprises Inc is recalling DrugCheck 8 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP Product Code 60800 due to Label lacks professional use legend and name and address of the manufacturer.. Based on FDA medical device recall database.
Summary derived from FDA notice
The following details were not provided by the FDA: specific lot/serial numbers.
Reason for Recall
As stated by FDA
Label lacks professional use legend and name and address of the manufacturer.
Recommended Action
Per FDA guidance
The firm sent a letter to customers requesting that they overlabel their stock on 3/20/2003. This recall is complete.
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