Device recall
Z-1256-03: DrugCheck 9 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP/MTD Product Code 60925
FDA device recall · Class III · Drug Free Enterprises Inc
Key facts
| Recall number (Z-number) | Z-1256-03 |
|---|---|
| Recall event | 27074 |
| Product | DrugCheck 9 Test Cup AMP/COC/OPI/THC/MET/BZD/BAR/PCP/MTD Product Code 60925 |
| Product code | DIO |
| Recalling firm | Drug Free Enterprises Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 22, 2003 |
| FEI number | 3003470018 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database