Drug recall
Leica ASP6025 Vacuum Tissue Processor The Leica ASP6025 is a modular tissue processor for the following…
FDA recall event 63935 · Class II · Leica Microsystems, Inc.
Key facts
| Event ID | 63935 |
|---|---|
| Recall numbers | Z-1815-2013 |
| Recalling firm | Leica Microsystems, Inc. |
| Product type | Devices |
| Products | Leica ASP6025 Vacuum Tissue Processor The Leica ASP6025 is a modular tissue processor for the following laboratory applications: fixation, dehydration, infiltration with intermedium, and the paraffin… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The Instruction for Use 1v9 Ref F and all previous versions specify incorrect dimensions for the Ready To Use (RTU) bottles from other suppliers than Leica. In case of a pressure failure of the device… |
| Initiation date | Nov 13, 2012 |
| Report date | Aug 7, 2013 |
| Termination date | Jan 5, 2017 |
| City | Buffalo Grove |
| State | IL |
| Country | United States |
| FEI number | 3000210133 |
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: