Drug recall
QIAGEN artus CMV RG PCR ASR (24) (Catalog number 4503223) Product Usage: The artus CMV RG PCR ASR is designed…
FDA recall event 64650 · Class II · QIAGEN Gaithersburg, Inc.
Key facts
| Event ID | 64650 |
|---|---|
| Recall numbers | Z-1320-2013, Z-1321-2013 |
| Recalling firm | QIAGEN Gaithersburg, Inc. |
| Product type | Devices |
| Products | 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…, QIAGEN artus CMV RG PCR ASR (96) (Catalog number 4503225) Product Usage: Test is intended for use in the detection and quantitation of human cytomegalovirus (CMV) specific DNA, as part of an in house… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | CMV RG PCR kits may contain a mixture of incorrect vials among the correct vials. |
| Initiation date | Jan 30, 2013 |
| Report date | May 22, 2013 |
| Termination date | Jul 1, 2013 |
| City | Gaithersburg |
| State | MD |
| Country | United States |
| FEI number | 1122376 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: