Device recall
Z-1457-2011: QuickVue One-Step hCG Urine, Quidel Catalog Number: 20109, Lot Number: 706842
FDA device recall · Class II · Quidel Corporation
Key facts
| Recall number (Z-number) | Z-1457-2011 |
|---|---|
| Recall event | 57402 |
| Product | QuickVue One-Step hCG Urine, Quidel Catalog Number: 20109, Lot Number: 706842 |
| Product code | JHI |
| Recalling firm | Quidel Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 26, 2012 |
| 510(k) numbers | K020799 |
| FEI number | 2024674 |
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