Drug recall
Power Processor 1K Stockyard. The Power Processor performs all pre-analytical sample tube preparation.
FDA recall event 77982 · Class II · Beckman Coulter Inc.
Key facts
| Event ID | 77982 |
|---|---|
| Recall numbers | Z-0046-2018 |
| Recalling firm | Beckman Coulter Inc. |
| Product type | Devices |
| Products | Power Processor 1K Stockyard. The Power Processor performs all pre-analytical sample tube preparation. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Beckman Coulter has identified that due to a PLC software nonconformity the 1K Stockyard can initiate a retrieval of a sample tube during the rack loading process, which should not occur. This issue… |
| Initiation date | Aug 3, 2017 |
| Report date | Nov 1, 2017 |
| Termination date | Sep 27, 2023 |
| City | Brea |
| State | CA |
| Country | United States |
| FEI number | 2050012 |
At a glance
- 1–9 Products in this recall
- 10–99 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: