FDA Medical Device Recalls (openFDA)
Drug Free Enterprises Inc: DrugCheck 9 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP/TCA Product Code 60900
- Recall number
- Z-1254-03
- Recalling firm
- Drug Free Enterprises Inc
- Product
- DrugCheck 9 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP/TCA Product Code 60900
- Status
- Terminated
- Initiated
- 2003-03-20
- Posted
- 2003-09-23
- Terminated
- 2003-09-22
- Reason
- Label lacks professional use legend and name and address of the manufacturer.
- Root cause
- Other
- Action
- The firm sent a letter to customers requesting that they overlabel their stock on 3/20/2003. This recall is complete.
- Quantity
- Undetermined.
- Distribution
- Nationwide
- Lot, serial or model codes
- All
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- DIO
- Firm FEI
- 3003470018
- Firm city
- Agoura Hills
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28