Device recall
Z-1086-2012: UltraVision Large Volume Detection System; Anti-Polyvalent, Alk-Phos (Ready to…
FDA device recall · Class II · Lab Vision Corporation
Key facts
| Recall number (Z-number) | Z-1086-2012 |
|---|---|
| Recall event | 60967 |
| Product | UltraVision Large Volume Detection System; Anti-Polyvalent, Alk-Phos (Ready to Use) Manufactured by: Lab Vision Corporation 46360 Fremont Blvd, Fremont, CA 94538 Product Usage: These products detect specific antibodies bound to an antigen in tissue sections. The specific antibody is located by a… |
| Product code | NJT |
| Recalling firm | Lab Vision Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 20, 2012 |
| FEI number | 3000719701 |
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