Device recall
Z-0950-03: Bindazyme, Human AntiCardiolipin IgM Enzyme Immunoassay Kits, MK029
FDA device recall · Class III · Binding Site Inc The
Key facts
| Recall number (Z-number) | Z-0950-03 |
|---|---|
| Recall event | 26433 |
| Product | Bindazyme, Human AntiCardiolipin IgM Enzyme Immunoassay Kits, MK029 |
| Product code | MID |
| Recalling firm | Binding Site Inc The |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 1, 2004 |
| 510(k) numbers | K983694 |
| FEI number | 2083566 |
At a glance
- 1–9 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