Drug recall
ARIES System and ARIES M1 System
FDA recall event 77052 · Class II · Luminex Corporation
Key facts
| Event ID | 77052 |
|---|---|
| Recall numbers | Z-2094-2017 |
| Recalling firm | Luminex Corporation |
| Product type | Devices |
| Products | ARIES System and ARIES M1 System |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The hand-held barcode scanner that is used as an accessory to enter ARIES cassette and specimen identifications on the ARIES Systems populates patient sample IDs with a previously scanned sample ID… |
| Initiation date | Apr 19, 2017 |
| Report date | May 24, 2017 |
| Termination date | Oct 20, 2017 |
| City | Austin |
| State | TX |
| Country | United States |
| FEI number | 3002524000 |
At a glance
- 1–9 Products in this recall
- 1–9 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: