Device recall
Z-0961-03: Measles (Rubeola) IgG ELISA Test System. It is an enzyme-linked immunosorbent…
FDA device recall · Class III · Zeus Scientific Inc
Key facts
| Recall number (Z-number) | Z-0961-03 |
|---|---|
| Recall event | 26402 |
| Product | Measles (Rubeola) IgG ELISA Test System. It is an enzyme-linked immunosorbent assay (ELISA) designed for the qualitative detection of IgG antibodies to Measles (Rubeola) virus in human serum and is for in vitro diagnostic use. Product Number: 507055 |
| Product code | LJB |
| Recalling firm | Zeus Scientific Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 3, 2006 |
| FEI number | 2242436 |
At a glance
- None 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