Device recall
Z-2779-2015: The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology…
FDA device recall · Class III · Leica Microsystems, Inc.
Key facts
| Recall number (Z-number) | Z-2779-2015 |
|---|---|
| Recall event | 71910 |
| Product | The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology Departments. The Leica ASP200S/ASP300S Tissue Processor is an automated system used to process tissue specimens for examination through fixation, dehydration and infiltration. |
| Product code | IEO |
| Recalling firm | Leica Microsystems, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 5, 2017 |
| FEI number | 3000210133 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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