Drug Check 4 Test Cup AMP/COC/OPI/THC Product Code 60400, and 60410
FDA device recall Z-1246-03 · 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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