Device recall
Z-0239-04: DrugCheck 5, in-vitro diagnostic test for drugs of abuse: AMP, COC, THC, OPI…
FDA device recall · Class III · Drug Free Enterprises Inc
Key facts
| Recall number (Z-number) | Z-0239-04 |
|---|---|
| Recall event | 27817 |
| Product | DrugCheck 5, in-vitro diagnostic test for drugs of abuse: AMP, COC, THC, OPI, MET. |
| Product code | DIO |
| Recalling firm | Drug Free Enterprises Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 17, 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