Device recall
Z-1095-03: Cytomegalovirus (CMV) IgG ELISA Test System, In-Vitro Diagnostic, manufactured…
FDA device recall · Class II · Zeus Scientific Inc
Key facts
| Recall number (Z-number) | Z-1095-03 |
|---|---|
| Recall event | 26589 |
| Product | Cytomegalovirus (CMV) IgG ELISA Test System, In-Vitro Diagnostic, manufactured by Zeus Scientific, Inc., Raritan, NJ. |
| Product code | LFZ |
| Recalling firm | Zeus Scientific Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 22, 2006 |
| 510(k) numbers | K891081 |
| FEI number | 2242436 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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