Device recall
Z-2050-2020: Professional Urine Drug Control, Item code 88010 - Product Usage: The Alere…
FDA device recall · Class II · Cardinal Health Inc.
Key facts
| Recall number (Z-number) | Z-2050-2020 |
|---|---|
| Recall event | 85509 |
| Product | Professional Urine Drug Control, Item code 88010 - Product Usage: The Alere Professional Cup Urine Drug Controls are compatible with all quantitative and qualitative drug detection procedures which are sufficiently sensitive to detect the control constituents. |
| Product code | JJW |
| Recalling firm | Cardinal Health Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 23, 2020 |
| FEI number | 3004008697 |
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