Device recall
Z-1552-2020: Quidel Triage TOX Drug Screen Control 1 Kit Box containing 5 Control 1 vials…
FDA device recall · Class II · QUIDEL CARDIOVASCULAR INC
Key facts
| Recall number (Z-number) | Z-1552-2020 |
|---|---|
| Recall event | 84698 |
| Product | Quidel Triage TOX Drug Screen Control 1 Kit Box containing 5 Control 1 vials with 5 x 0.25 mL vials per box. Quidel Cardiovascular Inc. 9975 Summers Ridge Road San Diego, CA 92121 USA Quidel.com |
| Product code | DIF |
| Recalling firm | QUIDEL CARDIOVASCULAR INC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 14, 2021 |
| 510(k) numbers | K060788 |
| FEI number | 3013982035 |
At a glance
- 1–9 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