Device recall
Z-1202-03: On-Site Alcohol IVD A single use enzymatic assay for qualitative detection of…
FDA device recall · Class III · Varian, Inc.
Key facts
| Recall number (Z-number) | Z-1202-03 |
|---|---|
| Recall event | 26829 |
| Product | On-Site Alcohol IVD A single use enzymatic assay for qualitative detection of alcohol in urine or saliva. Catalog numbers: 47464 Roche Diagnostics Label A305-02 Varian, Inc. label |
| Product code | DML |
| Recalling firm | Varian, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 17, 2004 |
| FEI number | 2026835 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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