Device recall
Z-0270-2019: Accutest Drug Test Cup 5+3 Product Usage: The Accutest Drug Test Cup is an in…
FDA device recall · Class III · Ameditech Inc
Key facts
| Recall number (Z-number) | Z-0270-2019 |
|---|---|
| Recall event | 80861 |
| Product | Accutest Drug Test Cup 5+3 Product Usage: The Accutest Drug Test Cup is an in vitro diagnostic test for the rapid detection of multiple drugs in human urine. The test is intended as the first step in a two-step process to provide consumers with information concerning the presence or absence of drugs… |
| Product code | NGG |
| Recalling firm | Ameditech Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 6, 2019 |
| 510(k) numbers | K082898 |
| FEI number | 3003789989 |
At a glance
- 1–9 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