Device recall
Z-1321-2013: QIAGEN artus CMV RG PCR ASR (24) (Catalog number 4503223) Product Usage: The…
FDA device recall · Class II · QIAGEN Gaithersburg, Inc.
Key facts
| Recall number (Z-number) | Z-1321-2013 |
|---|---|
| Recall event | 64650 |
| Product | QIAGEN artus CMV RG PCR ASR (24) (Catalog number 4503223) Product Usage: The artus CMV RG PCR ASR is designed to detect and to quantify nucleic acid specific to human cytomegalovirus (CMV) using real-time PCR technology (PCR) in the Rotor-Gene 2000/3000 (RG). |
| Product code | LKQ |
| Recalling firm | QIAGEN Gaithersburg, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 1, 2013 |
| FEI number | 3003572099 |
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